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1.

rs1491557319 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    CA>- [Show Flanks]
    Chromosome:
    10:96025363 (GRCh38)
    10:97785120 (GRCh37)
    Canonical SPDI:
    NC_000010.11:96025362:CA:
    Gene:
    CC2D2B (Varview), ENTPD1-AS1 (Varview)
    Functional Consequence:
    downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    -=0./0 (ALFA)
    HGVS:

    2.

    rs1491530126 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CA>- [Show Flanks]
      Chromosome:
      10:95879787 (GRCh38)
      10:97639544 (GRCh37)
      Canonical SPDI:
      NC_000010.11:95879786:CA:
      Gene:
      ENTPD1-AS1 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      -=0.00792/94 (ALFA)
      -=0.00277/78 (TOMMO)
      HGVS:

      3.

      rs1491497062 has merged into rs11312564 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        10:95869251 (GRCh38)
        10:97629008 (GRCh37)
        Canonical SPDI:
        NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        ENTPD1 (Varview), ENTPD1-AS1 (Varview)
        Functional Consequence:
        intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTTTTTTTT=0./0 (ALFA)
        HGVS:
        NC_000010.11:g.95869251_95869267del, NC_000010.11:g.95869253_95869267del, NC_000010.11:g.95869254_95869267del, NC_000010.11:g.95869255_95869267del, NC_000010.11:g.95869256_95869267del, NC_000010.11:g.95869257_95869267del, NC_000010.11:g.95869258_95869267del, NC_000010.11:g.95869259_95869267del, NC_000010.11:g.95869260_95869267del, NC_000010.11:g.95869261_95869267del, NC_000010.11:g.95869262_95869267del, NC_000010.11:g.95869263_95869267del, NC_000010.11:g.95869264_95869267del, NC_000010.11:g.95869265_95869267del, NC_000010.11:g.95869266_95869267del, NC_000010.11:g.95869267del, NC_000010.11:g.95869267dup, NC_000010.11:g.95869266_95869267dup, NC_000010.11:g.95869265_95869267dup, NC_000010.11:g.95869264_95869267dup, NC_000010.11:g.95869263_95869267dup, NC_000010.11:g.95869262_95869267dup, NC_000010.11:g.95869261_95869267dup, NC_000010.11:g.95869260_95869267dup, NC_000010.11:g.95869258_95869267dup, NC_000010.11:g.95869256_95869267dup, NC_000010.11:g.95869255_95869267dup, NC_000010.11:g.95869253_95869267dup, NC_000010.11:g.95869252_95869267dup, NC_000010.11:g.95869251_95869267dup, NC_000010.11:g.95869248_95869267dup, NC_000010.11:g.95869247_95869267dup, NC_000010.11:g.95869246_95869267dup, NC_000010.11:g.95869245_95869267dup, NC_000010.11:g.95869244_95869267dup, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629008_97629024del, NC_000010.10:g.97629010_97629024del, NC_000010.10:g.97629011_97629024del, NC_000010.10:g.97629012_97629024del, NC_000010.10:g.97629013_97629024del, NC_000010.10:g.97629014_97629024del, NC_000010.10:g.97629015_97629024del, NC_000010.10:g.97629016_97629024del, NC_000010.10:g.97629017_97629024del, NC_000010.10:g.97629018_97629024del, NC_000010.10:g.97629019_97629024del, NC_000010.10:g.97629020_97629024del, NC_000010.10:g.97629021_97629024del, NC_000010.10:g.97629022_97629024del, NC_000010.10:g.97629023_97629024del, NC_000010.10:g.97629024del, NC_000010.10:g.97629024dup, NC_000010.10:g.97629023_97629024dup, NC_000010.10:g.97629022_97629024dup, NC_000010.10:g.97629021_97629024dup, NC_000010.10:g.97629020_97629024dup, NC_000010.10:g.97629019_97629024dup, NC_000010.10:g.97629018_97629024dup, NC_000010.10:g.97629017_97629024dup, NC_000010.10:g.97629015_97629024dup, NC_000010.10:g.97629013_97629024dup, NC_000010.10:g.97629012_97629024dup, NC_000010.10:g.97629010_97629024dup, NC_000010.10:g.97629009_97629024dup, NC_000010.10:g.97629008_97629024dup, NC_000010.10:g.97629005_97629024dup, NC_000010.10:g.97629004_97629024dup, NC_000010.10:g.97629003_97629024dup, NC_000010.10:g.97629002_97629024dup, NC_000010.10:g.97629001_97629024dup, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162473_162489del, NG_042803.1:g.162475_162489del, NG_042803.1:g.162476_162489del, NG_042803.1:g.162477_162489del, NG_042803.1:g.162478_162489del, NG_042803.1:g.162479_162489del, NG_042803.1:g.162480_162489del, NG_042803.1:g.162481_162489del, NG_042803.1:g.162482_162489del, NG_042803.1:g.162483_162489del, NG_042803.1:g.162484_162489del, NG_042803.1:g.162485_162489del, NG_042803.1:g.162486_162489del, NG_042803.1:g.162487_162489del, NG_042803.1:g.162488_162489del, NG_042803.1:g.162489del, NG_042803.1:g.162489dup, NG_042803.1:g.162488_162489dup, NG_042803.1:g.162487_162489dup, NG_042803.1:g.162486_162489dup, NG_042803.1:g.162485_162489dup, NG_042803.1:g.162484_162489dup, NG_042803.1:g.162483_162489dup, NG_042803.1:g.162482_162489dup, NG_042803.1:g.162480_162489dup, NG_042803.1:g.162478_162489dup, NG_042803.1:g.162477_162489dup, NG_042803.1:g.162475_162489dup, NG_042803.1:g.162474_162489dup, NG_042803.1:g.162473_162489dup, NG_042803.1:g.162470_162489dup, NG_042803.1:g.162469_162489dup, NG_042803.1:g.162468_162489dup, NG_042803.1:g.162467_162489dup, NG_042803.1:g.162466_162489dup, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2868_*2884del, NM_001776.6:c.*2870_*2884del, NM_001776.6:c.*2871_*2884del, NM_001776.6:c.*2872_*2884del, NM_001776.6:c.*2873_*2884del, NM_001776.6:c.*2874_*2884del, NM_001776.6:c.*2875_*2884del, NM_001776.6:c.*2876_*2884del, NM_001776.6:c.*2877_*2884del, NM_001776.6:c.*2878_*2884del, NM_001776.6:c.*2879_*2884del, NM_001776.6:c.*2880_*2884del, NM_001776.6:c.*2881_*2884del, NM_001776.6:c.*2882_*2884del, NM_001776.6:c.*2883_*2884del, NM_001776.6:c.*2884del, NM_001776.6:c.*2884dup, NM_001776.6:c.*2883_*2884dup, NM_001776.6:c.*2882_*2884dup, NM_001776.6:c.*2881_*2884dup, NM_001776.6:c.*2880_*2884dup, NM_001776.6:c.*2879_*2884dup, NM_001776.6:c.*2878_*2884dup, NM_001776.6:c.*2877_*2884dup, NM_001776.6:c.*2875_*2884dup, NM_001776.6:c.*2873_*2884dup, NM_001776.6:c.*2872_*2884dup, NM_001776.6:c.*2870_*2884dup, NM_001776.6:c.*2869_*2884dup, NM_001776.6:c.*2868_*2884dup, NM_001776.6:c.*2865_*2884dup, NM_001776.6:c.*2864_*2884dup, NM_001776.6:c.*2863_*2884dup, NM_001776.6:c.*2862_*2884dup, NM_001776.6:c.*2861_*2884dup, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2868_*2884del, NM_001776.5:c.*2870_*2884del, NM_001776.5:c.*2871_*2884del, NM_001776.5:c.*2872_*2884del, NM_001776.5:c.*2873_*2884del, NM_001776.5:c.*2874_*2884del, NM_001776.5:c.*2875_*2884del, NM_001776.5:c.*2876_*2884del, NM_001776.5:c.*2877_*2884del, NM_001776.5:c.*2878_*2884del, NM_001776.5:c.*2879_*2884del, NM_001776.5:c.*2880_*2884del, NM_001776.5:c.*2881_*2884del, NM_001776.5:c.*2882_*2884del, NM_001776.5:c.*2883_*2884del, NM_001776.5:c.*2884del, NM_001776.5:c.*2884dup, NM_001776.5:c.*2883_*2884dup, NM_001776.5:c.*2882_*2884dup, NM_001776.5:c.*2881_*2884dup, NM_001776.5:c.*2880_*2884dup, NM_001776.5:c.*2879_*2884dup, NM_001776.5:c.*2878_*2884dup, NM_001776.5:c.*2877_*2884dup, NM_001776.5:c.*2875_*2884dup, NM_001776.5:c.*2873_*2884dup, NM_001776.5:c.*2872_*2884dup, NM_001776.5:c.*2870_*2884dup, NM_001776.5:c.*2869_*2884dup, NM_001776.5:c.*2868_*2884dup, NM_001776.5:c.*2865_*2884dup, NM_001776.5:c.*2864_*2884dup, NM_001776.5:c.*2863_*2884dup, NM_001776.5:c.*2862_*2884dup, NM_001776.5:c.*2861_*2884dup, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2868_*2884del, NM_001098175.2:c.*2870_*2884del, NM_001098175.2:c.*2871_*2884del, NM_001098175.2:c.*2872_*2884del, NM_001098175.2:c.*2873_*2884del, NM_001098175.2:c.*2874_*2884del, NM_001098175.2:c.*2875_*2884del, NM_001098175.2:c.*2876_*2884del, NM_001098175.2:c.*2877_*2884del, NM_001098175.2:c.*2878_*2884del, NM_001098175.2:c.*2879_*2884del, NM_001098175.2:c.*2880_*2884del, NM_001098175.2:c.*2881_*2884del, NM_001098175.2:c.*2882_*2884del, NM_001098175.2:c.*2883_*2884del, NM_001098175.2:c.*2884del, NM_001098175.2:c.*2884dup, NM_001098175.2:c.*2883_*2884dup, NM_001098175.2:c.*2882_*2884dup, NM_001098175.2:c.*2881_*2884dup, NM_001098175.2:c.*2880_*2884dup, NM_001098175.2:c.*2879_*2884dup, NM_001098175.2:c.*2878_*2884dup, NM_001098175.2:c.*2877_*2884dup, NM_001098175.2:c.*2875_*2884dup, NM_001098175.2:c.*2873_*2884dup, NM_001098175.2:c.*2872_*2884dup, NM_001098175.2:c.*2870_*2884dup, NM_001098175.2:c.*2869_*2884dup, NM_001098175.2:c.*2868_*2884dup, NM_001098175.2:c.*2865_*2884dup, NM_001098175.2:c.*2864_*2884dup, NM_001098175.2:c.*2863_*2884dup, NM_001098175.2:c.*2862_*2884dup, NM_001098175.2:c.*2861_*2884dup, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2868_*2884del, NM_001098175.1:c.*2870_*2884del, NM_001098175.1:c.*2871_*2884del, NM_001098175.1:c.*2872_*2884del, NM_001098175.1:c.*2873_*2884del, NM_001098175.1:c.*2874_*2884del, NM_001098175.1:c.*2875_*2884del, NM_001098175.1:c.*2876_*2884del, NM_001098175.1:c.*2877_*2884del, NM_001098175.1:c.*2878_*2884del, NM_001098175.1:c.*2879_*2884del, NM_001098175.1:c.*2880_*2884del, NM_001098175.1:c.*2881_*2884del, NM_001098175.1:c.*2882_*2884del, NM_001098175.1:c.*2883_*2884del, NM_001098175.1:c.*2884del, NM_001098175.1:c.*2884dup, NM_001098175.1:c.*2883_*2884dup, NM_001098175.1:c.*2882_*2884dup, NM_001098175.1:c.*2881_*2884dup, NM_001098175.1:c.*2880_*2884dup, NM_001098175.1:c.*2879_*2884dup, NM_001098175.1:c.*2878_*2884dup, NM_001098175.1:c.*2877_*2884dup, NM_001098175.1:c.*2875_*2884dup, NM_001098175.1:c.*2873_*2884dup, NM_001098175.1:c.*2872_*2884dup, NM_001098175.1:c.*2870_*2884dup, NM_001098175.1:c.*2869_*2884dup, NM_001098175.1:c.*2868_*2884dup, NM_001098175.1:c.*2865_*2884dup, NM_001098175.1:c.*2864_*2884dup, NM_001098175.1:c.*2863_*2884dup, NM_001098175.1:c.*2862_*2884dup, NM_001098175.1:c.*2861_*2884dup, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2868_*2884del, NM_001164179.2:c.*2870_*2884del, NM_001164179.2:c.*2871_*2884del, NM_001164179.2:c.*2872_*2884del, NM_001164179.2:c.*2873_*2884del, NM_001164179.2:c.*2874_*2884del, NM_001164179.2:c.*2875_*2884del, NM_001164179.2:c.*2876_*2884del, NM_001164179.2:c.*2877_*2884del, NM_001164179.2:c.*2878_*2884del, NM_001164179.2:c.*2879_*2884del, NM_001164179.2:c.*2880_*2884del, NM_001164179.2:c.*2881_*2884del, NM_001164179.2:c.*2882_*2884del, NM_001164179.2:c.*2883_*2884del, NM_001164179.2:c.*2884del, NM_001164179.2:c.*2884dup, NM_001164179.2:c.*2883_*2884dup, NM_001164179.2:c.*2882_*2884dup, NM_001164179.2:c.*2881_*2884dup, NM_001164179.2:c.*2880_*2884dup, NM_001164179.2:c.*2879_*2884dup, NM_001164179.2:c.*2878_*2884dup, NM_001164179.2:c.*2877_*2884dup, NM_001164179.2:c.*2875_*2884dup, NM_001164179.2:c.*2873_*2884dup, NM_001164179.2:c.*2872_*2884dup, NM_001164179.2:c.*2870_*2884dup, NM_001164179.2:c.*2869_*2884dup, NM_001164179.2:c.*2868_*2884dup, NM_001164179.2:c.*2865_*2884dup, NM_001164179.2:c.*2864_*2884dup, NM_001164179.2:c.*2863_*2884dup, NM_001164179.2:c.*2862_*2884dup, NM_001164179.2:c.*2861_*2884dup, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2868_*2884del, NM_001164179.1:c.*2870_*2884del, NM_001164179.1:c.*2871_*2884del, NM_001164179.1:c.*2872_*2884del, NM_001164179.1:c.*2873_*2884del, NM_001164179.1:c.*2874_*2884del, NM_001164179.1:c.*2875_*2884del, NM_001164179.1:c.*2876_*2884del, NM_001164179.1:c.*2877_*2884del, NM_001164179.1:c.*2878_*2884del, NM_001164179.1:c.*2879_*2884del, NM_001164179.1:c.*2880_*2884del, NM_001164179.1:c.*2881_*2884del, NM_001164179.1:c.*2882_*2884del, NM_001164179.1:c.*2883_*2884del, NM_001164179.1:c.*2884del, NM_001164179.1:c.*2884dup, NM_001164179.1:c.*2883_*2884dup, NM_001164179.1:c.*2882_*2884dup, NM_001164179.1:c.*2881_*2884dup, NM_001164179.1:c.*2880_*2884dup, NM_001164179.1:c.*2879_*2884dup, NM_001164179.1:c.*2878_*2884dup, NM_001164179.1:c.*2877_*2884dup, NM_001164179.1:c.*2875_*2884dup, NM_001164179.1:c.*2873_*2884dup, NM_001164179.1:c.*2872_*2884dup, NM_001164179.1:c.*2870_*2884dup, NM_001164179.1:c.*2869_*2884dup, NM_001164179.1:c.*2868_*2884dup, NM_001164179.1:c.*2865_*2884dup, NM_001164179.1:c.*2864_*2884dup, NM_001164179.1:c.*2863_*2884dup, NM_001164179.1:c.*2862_*2884dup, NM_001164179.1:c.*2861_*2884dup, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2868_*2884del, NM_001164182.2:c.*2870_*2884del, NM_001164182.2:c.*2871_*2884del, NM_001164182.2:c.*2872_*2884del, NM_001164182.2:c.*2873_*2884del, NM_001164182.2:c.*2874_*2884del, NM_001164182.2:c.*2875_*2884del, NM_001164182.2:c.*2876_*2884del, NM_001164182.2:c.*2877_*2884del, NM_001164182.2:c.*2878_*2884del, NM_001164182.2:c.*2879_*2884del, NM_001164182.2:c.*2880_*2884del, NM_001164182.2:c.*2881_*2884del, NM_001164182.2:c.*2882_*2884del, NM_001164182.2:c.*2883_*2884del, NM_001164182.2:c.*2884del, NM_001164182.2:c.*2884dup, NM_001164182.2:c.*2883_*2884dup, NM_001164182.2:c.*2882_*2884dup, NM_001164182.2:c.*2881_*2884dup, NM_001164182.2:c.*2880_*2884dup, NM_001164182.2:c.*2879_*2884dup, NM_001164182.2:c.*2878_*2884dup, NM_001164182.2:c.*2877_*2884dup, NM_001164182.2:c.*2875_*2884dup, NM_001164182.2:c.*2873_*2884dup, NM_001164182.2:c.*2872_*2884dup, NM_001164182.2:c.*2870_*2884dup, NM_001164182.2:c.*2869_*2884dup, NM_001164182.2:c.*2868_*2884dup, NM_001164182.2:c.*2865_*2884dup, NM_001164182.2:c.*2864_*2884dup, NM_001164182.2:c.*2863_*2884dup, NM_001164182.2:c.*2862_*2884dup, NM_001164182.2:c.*2861_*2884dup, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2868_*2884del, NM_001164182.1:c.*2870_*2884del, NM_001164182.1:c.*2871_*2884del, NM_001164182.1:c.*2872_*2884del, NM_001164182.1:c.*2873_*2884del, NM_001164182.1:c.*2874_*2884del, NM_001164182.1:c.*2875_*2884del, NM_001164182.1:c.*2876_*2884del, NM_001164182.1:c.*2877_*2884del, NM_001164182.1:c.*2878_*2884del, NM_001164182.1:c.*2879_*2884del, NM_001164182.1:c.*2880_*2884del, NM_001164182.1:c.*2881_*2884del, NM_001164182.1:c.*2882_*2884del, NM_001164182.1:c.*2883_*2884del, NM_001164182.1:c.*2884del, NM_001164182.1:c.*2884dup, NM_001164182.1:c.*2883_*2884dup, NM_001164182.1:c.*2882_*2884dup, NM_001164182.1:c.*2881_*2884dup, NM_001164182.1:c.*2880_*2884dup, NM_001164182.1:c.*2879_*2884dup, NM_001164182.1:c.*2878_*2884dup, NM_001164182.1:c.*2877_*2884dup, NM_001164182.1:c.*2875_*2884dup, NM_001164182.1:c.*2873_*2884dup, NM_001164182.1:c.*2872_*2884dup, NM_001164182.1:c.*2870_*2884dup, NM_001164182.1:c.*2869_*2884dup, NM_001164182.1:c.*2868_*2884dup, NM_001164182.1:c.*2865_*2884dup, NM_001164182.1:c.*2864_*2884dup, NM_001164182.1:c.*2863_*2884dup, NM_001164182.1:c.*2862_*2884dup, NM_001164182.1:c.*2861_*2884dup, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2868_*2884del, NM_001164183.2:c.*2870_*2884del, NM_001164183.2:c.*2871_*2884del, NM_001164183.2:c.*2872_*2884del, NM_001164183.2:c.*2873_*2884del, NM_001164183.2:c.*2874_*2884del, NM_001164183.2:c.*2875_*2884del, NM_001164183.2:c.*2876_*2884del, NM_001164183.2:c.*2877_*2884del, NM_001164183.2:c.*2878_*2884del, NM_001164183.2:c.*2879_*2884del, NM_001164183.2:c.*2880_*2884del, NM_001164183.2:c.*2881_*2884del, NM_001164183.2:c.*2882_*2884del, NM_001164183.2:c.*2883_*2884del, NM_001164183.2:c.*2884del, NM_001164183.2:c.*2884dup, NM_001164183.2:c.*2883_*2884dup, NM_001164183.2:c.*2882_*2884dup, NM_001164183.2:c.*2881_*2884dup, NM_001164183.2:c.*2880_*2884dup, NM_001164183.2:c.*2879_*2884dup, NM_001164183.2:c.*2878_*2884dup, NM_001164183.2:c.*2877_*2884dup, NM_001164183.2:c.*2875_*2884dup, NM_001164183.2:c.*2873_*2884dup, NM_001164183.2:c.*2872_*2884dup, NM_001164183.2:c.*2870_*2884dup, NM_001164183.2:c.*2869_*2884dup, NM_001164183.2:c.*2868_*2884dup, NM_001164183.2:c.*2865_*2884dup, NM_001164183.2:c.*2864_*2884dup, NM_001164183.2:c.*2863_*2884dup, NM_001164183.2:c.*2862_*2884dup, NM_001164183.2:c.*2861_*2884dup, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2868_*2884del, NM_001164183.1:c.*2870_*2884del, NM_001164183.1:c.*2871_*2884del, NM_001164183.1:c.*2872_*2884del, NM_001164183.1:c.*2873_*2884del, NM_001164183.1:c.*2874_*2884del, NM_001164183.1:c.*2875_*2884del, NM_001164183.1:c.*2876_*2884del, NM_001164183.1:c.*2877_*2884del, NM_001164183.1:c.*2878_*2884del, NM_001164183.1:c.*2879_*2884del, NM_001164183.1:c.*2880_*2884del, NM_001164183.1:c.*2881_*2884del, NM_001164183.1:c.*2882_*2884del, NM_001164183.1:c.*2883_*2884del, NM_001164183.1:c.*2884del, NM_001164183.1:c.*2884dup, NM_001164183.1:c.*2883_*2884dup, NM_001164183.1:c.*2882_*2884dup, NM_001164183.1:c.*2881_*2884dup, NM_001164183.1:c.*2880_*2884dup, NM_001164183.1:c.*2879_*2884dup, NM_001164183.1:c.*2878_*2884dup, NM_001164183.1:c.*2877_*2884dup, NM_001164183.1:c.*2875_*2884dup, NM_001164183.1:c.*2873_*2884dup, NM_001164183.1:c.*2872_*2884dup, NM_001164183.1:c.*2870_*2884dup, NM_001164183.1:c.*2869_*2884dup, NM_001164183.1:c.*2868_*2884dup, NM_001164183.1:c.*2865_*2884dup, NM_001164183.1:c.*2864_*2884dup, NM_001164183.1:c.*2863_*2884dup, NM_001164183.1:c.*2862_*2884dup, NM_001164183.1:c.*2861_*2884dup, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2868_*2884del, NM_001312654.1:c.*2870_*2884del, NM_001312654.1:c.*2871_*2884del, NM_001312654.1:c.*2872_*2884del, NM_001312654.1:c.*2873_*2884del, NM_001312654.1:c.*2874_*2884del, NM_001312654.1:c.*2875_*2884del, NM_001312654.1:c.*2876_*2884del, NM_001312654.1:c.*2877_*2884del, NM_001312654.1:c.*2878_*2884del, NM_001312654.1:c.*2879_*2884del, NM_001312654.1:c.*2880_*2884del, NM_001312654.1:c.*2881_*2884del, NM_001312654.1:c.*2882_*2884del, NM_001312654.1:c.*2883_*2884del, NM_001312654.1:c.*2884del, NM_001312654.1:c.*2884dup, NM_001312654.1:c.*2883_*2884dup, NM_001312654.1:c.*2882_*2884dup, NM_001312654.1:c.*2881_*2884dup, NM_001312654.1:c.*2880_*2884dup, NM_001312654.1:c.*2879_*2884dup, NM_001312654.1:c.*2878_*2884dup, NM_001312654.1:c.*2877_*2884dup, NM_001312654.1:c.*2875_*2884dup, NM_001312654.1:c.*2873_*2884dup, NM_001312654.1:c.*2872_*2884dup, NM_001312654.1:c.*2870_*2884dup, NM_001312654.1:c.*2869_*2884dup, NM_001312654.1:c.*2868_*2884dup, NM_001312654.1:c.*2865_*2884dup, NM_001312654.1:c.*2864_*2884dup, NM_001312654.1:c.*2863_*2884dup, NM_001312654.1:c.*2862_*2884dup, NM_001312654.1:c.*2861_*2884dup, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2868_*2884del, NM_001164178.1:c.*2870_*2884del, NM_001164178.1:c.*2871_*2884del, NM_001164178.1:c.*2872_*2884del, NM_001164178.1:c.*2873_*2884del, NM_001164178.1:c.*2874_*2884del, NM_001164178.1:c.*2875_*2884del, NM_001164178.1:c.*2876_*2884del, NM_001164178.1:c.*2877_*2884del, NM_001164178.1:c.*2878_*2884del, NM_001164178.1:c.*2879_*2884del, NM_001164178.1:c.*2880_*2884del, NM_001164178.1:c.*2881_*2884del, NM_001164178.1:c.*2882_*2884del, NM_001164178.1:c.*2883_*2884del, NM_001164178.1:c.*2884del, NM_001164178.1:c.*2884dup, NM_001164178.1:c.*2883_*2884dup, NM_001164178.1:c.*2882_*2884dup, NM_001164178.1:c.*2881_*2884dup, NM_001164178.1:c.*2880_*2884dup, NM_001164178.1:c.*2879_*2884dup, NM_001164178.1:c.*2878_*2884dup, NM_001164178.1:c.*2877_*2884dup, NM_001164178.1:c.*2875_*2884dup, NM_001164178.1:c.*2873_*2884dup, NM_001164178.1:c.*2872_*2884dup, NM_001164178.1:c.*2870_*2884dup, NM_001164178.1:c.*2869_*2884dup, NM_001164178.1:c.*2868_*2884dup, NM_001164178.1:c.*2865_*2884dup, NM_001164178.1:c.*2864_*2884dup, NM_001164178.1:c.*2863_*2884dup, NM_001164178.1:c.*2862_*2884dup, NM_001164178.1:c.*2861_*2884dup, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2868_*2884del, NM_001164181.1:c.*2870_*2884del, NM_001164181.1:c.*2871_*2884del, NM_001164181.1:c.*2872_*2884del, NM_001164181.1:c.*2873_*2884del, NM_001164181.1:c.*2874_*2884del, NM_001164181.1:c.*2875_*2884del, NM_001164181.1:c.*2876_*2884del, NM_001164181.1:c.*2877_*2884del, NM_001164181.1:c.*2878_*2884del, NM_001164181.1:c.*2879_*2884del, NM_001164181.1:c.*2880_*2884del, NM_001164181.1:c.*2881_*2884del, NM_001164181.1:c.*2882_*2884del, NM_001164181.1:c.*2883_*2884del, NM_001164181.1:c.*2884del, NM_001164181.1:c.*2884dup, NM_001164181.1:c.*2883_*2884dup, NM_001164181.1:c.*2882_*2884dup, NM_001164181.1:c.*2881_*2884dup, NM_001164181.1:c.*2880_*2884dup, NM_001164181.1:c.*2879_*2884dup, NM_001164181.1:c.*2878_*2884dup, NM_001164181.1:c.*2877_*2884dup, NM_001164181.1:c.*2875_*2884dup, NM_001164181.1:c.*2873_*2884dup, NM_001164181.1:c.*2872_*2884dup, NM_001164181.1:c.*2870_*2884dup, NM_001164181.1:c.*2869_*2884dup, NM_001164181.1:c.*2868_*2884dup, NM_001164181.1:c.*2865_*2884dup, NM_001164181.1:c.*2864_*2884dup, NM_001164181.1:c.*2863_*2884dup, NM_001164181.1:c.*2862_*2884dup, NM_001164181.1:c.*2861_*2884dup, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2868_*2884del, XM_011540371.3:c.*2870_*2884del, XM_011540371.3:c.*2871_*2884del, XM_011540371.3:c.*2872_*2884del, XM_011540371.3:c.*2873_*2884del, XM_011540371.3:c.*2874_*2884del, XM_011540371.3:c.*2875_*2884del, XM_011540371.3:c.*2876_*2884del, XM_011540371.3:c.*2877_*2884del, XM_011540371.3:c.*2878_*2884del, XM_011540371.3:c.*2879_*2884del, XM_011540371.3:c.*2880_*2884del, XM_011540371.3:c.*2881_*2884del, XM_011540371.3:c.*2882_*2884del, XM_011540371.3:c.*2883_*2884del, XM_011540371.3:c.*2884del, XM_011540371.3:c.*2884dup, XM_011540371.3:c.*2883_*2884dup, XM_011540371.3:c.*2882_*2884dup, XM_011540371.3:c.*2881_*2884dup, XM_011540371.3:c.*2880_*2884dup, XM_011540371.3:c.*2879_*2884dup, XM_011540371.3:c.*2878_*2884dup, XM_011540371.3:c.*2877_*2884dup, XM_011540371.3:c.*2875_*2884dup, XM_011540371.3:c.*2873_*2884dup, XM_011540371.3:c.*2872_*2884dup, XM_011540371.3:c.*2870_*2884dup, XM_011540371.3:c.*2869_*2884dup, XM_011540371.3:c.*2868_*2884dup, XM_011540371.3:c.*2865_*2884dup, XM_011540371.3:c.*2864_*2884dup, XM_011540371.3:c.*2863_*2884dup, XM_011540371.3:c.*2862_*2884dup, XM_011540371.3:c.*2861_*2884dup, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2868_*2884del, XM_011540371.2:c.*2870_*2884del, XM_011540371.2:c.*2871_*2884del, XM_011540371.2:c.*2872_*2884del, XM_011540371.2:c.*2873_*2884del, XM_011540371.2:c.*2874_*2884del, XM_011540371.2:c.*2875_*2884del, XM_011540371.2:c.*2876_*2884del, XM_011540371.2:c.*2877_*2884del, XM_011540371.2:c.*2878_*2884del, XM_011540371.2:c.*2879_*2884del, XM_011540371.2:c.*2880_*2884del, XM_011540371.2:c.*2881_*2884del, XM_011540371.2:c.*2882_*2884del, XM_011540371.2:c.*2883_*2884del, XM_011540371.2:c.*2884del, XM_011540371.2:c.*2884dup, XM_011540371.2:c.*2883_*2884dup, XM_011540371.2:c.*2882_*2884dup, XM_011540371.2:c.*2881_*2884dup, XM_011540371.2:c.*2880_*2884dup, XM_011540371.2:c.*2879_*2884dup, XM_011540371.2:c.*2878_*2884dup, XM_011540371.2:c.*2877_*2884dup, XM_011540371.2:c.*2875_*2884dup, XM_011540371.2:c.*2873_*2884dup, XM_011540371.2:c.*2872_*2884dup, XM_011540371.2:c.*2870_*2884dup, XM_011540371.2:c.*2869_*2884dup, XM_011540371.2:c.*2868_*2884dup, XM_011540371.2:c.*2865_*2884dup, XM_011540371.2:c.*2864_*2884dup, XM_011540371.2:c.*2863_*2884dup, XM_011540371.2:c.*2862_*2884dup, XM_011540371.2:c.*2861_*2884dup, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2868_*2884del, XM_011540371.1:c.*2870_*2884del, XM_011540371.1:c.*2871_*2884del, XM_011540371.1:c.*2872_*2884del, XM_011540371.1:c.*2873_*2884del, XM_011540371.1:c.*2874_*2884del, XM_011540371.1:c.*2875_*2884del, XM_011540371.1:c.*2876_*2884del, XM_011540371.1:c.*2877_*2884del, XM_011540371.1:c.*2878_*2884del, XM_011540371.1:c.*2879_*2884del, XM_011540371.1:c.*2880_*2884del, XM_011540371.1:c.*2881_*2884del, XM_011540371.1:c.*2882_*2884del, XM_011540371.1:c.*2883_*2884del, XM_011540371.1:c.*2884del, XM_011540371.1:c.*2884dup, XM_011540371.1:c.*2883_*2884dup, XM_011540371.1:c.*2882_*2884dup, XM_011540371.1:c.*2881_*2884dup, XM_011540371.1:c.*2880_*2884dup, XM_011540371.1:c.*2879_*2884dup, XM_011540371.1:c.*2878_*2884dup, XM_011540371.1:c.*2877_*2884dup, XM_011540371.1:c.*2875_*2884dup, XM_011540371.1:c.*2873_*2884dup, XM_011540371.1:c.*2872_*2884dup, XM_011540371.1:c.*2870_*2884dup, XM_011540371.1:c.*2869_*2884dup, XM_011540371.1:c.*2868_*2884dup, XM_011540371.1:c.*2865_*2884dup, XM_011540371.1:c.*2864_*2884dup, XM_011540371.1:c.*2863_*2884dup, XM_011540371.1:c.*2862_*2884dup, XM_011540371.1:c.*2861_*2884dup, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2868_*2884del, XM_011540370.3:c.*2870_*2884del, XM_011540370.3:c.*2871_*2884del, XM_011540370.3:c.*2872_*2884del, XM_011540370.3:c.*2873_*2884del, XM_011540370.3:c.*2874_*2884del, XM_011540370.3:c.*2875_*2884del, XM_011540370.3:c.*2876_*2884del, XM_011540370.3:c.*2877_*2884del, XM_011540370.3:c.*2878_*2884del, XM_011540370.3:c.*2879_*2884del, XM_011540370.3:c.*2880_*2884del, XM_011540370.3:c.*2881_*2884del, XM_011540370.3:c.*2882_*2884del, XM_011540370.3:c.*2883_*2884del, XM_011540370.3:c.*2884del, XM_011540370.3:c.*2884dup, XM_011540370.3:c.*2883_*2884dup, XM_011540370.3:c.*2882_*2884dup, XM_011540370.3:c.*2881_*2884dup, XM_011540370.3:c.*2880_*2884dup, XM_011540370.3:c.*2879_*2884dup, XM_011540370.3:c.*2878_*2884dup, XM_011540370.3:c.*2877_*2884dup, XM_011540370.3:c.*2875_*2884dup, XM_011540370.3:c.*2873_*2884dup, XM_011540370.3:c.*2872_*2884dup, XM_011540370.3:c.*2870_*2884dup, XM_011540370.3:c.*2869_*2884dup, XM_011540370.3:c.*2868_*2884dup, XM_011540370.3:c.*2865_*2884dup, XM_011540370.3:c.*2864_*2884dup, XM_011540370.3:c.*2863_*2884dup, XM_011540370.3:c.*2862_*2884dup, XM_011540370.3:c.*2861_*2884dup, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2868_*2884del, XM_011540370.2:c.*2870_*2884del, XM_011540370.2:c.*2871_*2884del, XM_011540370.2:c.*2872_*2884del, XM_011540370.2:c.*2873_*2884del, XM_011540370.2:c.*2874_*2884del, XM_011540370.2:c.*2875_*2884del, XM_011540370.2:c.*2876_*2884del, XM_011540370.2:c.*2877_*2884del, XM_011540370.2:c.*2878_*2884del, XM_011540370.2:c.*2879_*2884del, XM_011540370.2:c.*2880_*2884del, XM_011540370.2:c.*2881_*2884del, XM_011540370.2:c.*2882_*2884del, XM_011540370.2:c.*2883_*2884del, XM_011540370.2:c.*2884del, XM_011540370.2:c.*2884dup, XM_011540370.2:c.*2883_*2884dup, XM_011540370.2:c.*2882_*2884dup, XM_011540370.2:c.*2881_*2884dup, XM_011540370.2:c.*2880_*2884dup, XM_011540370.2:c.*2879_*2884dup, XM_011540370.2:c.*2878_*2884dup, XM_011540370.2:c.*2877_*2884dup, XM_011540370.2:c.*2875_*2884dup, XM_011540370.2:c.*2873_*2884dup, XM_011540370.2:c.*2872_*2884dup, XM_011540370.2:c.*2870_*2884dup, XM_011540370.2:c.*2869_*2884dup, XM_011540370.2:c.*2868_*2884dup, XM_011540370.2:c.*2865_*2884dup, XM_011540370.2:c.*2864_*2884dup, XM_011540370.2:c.*2863_*2884dup, XM_011540370.2:c.*2862_*2884dup, XM_011540370.2:c.*2861_*2884dup, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2868_*2884del, XM_011540370.1:c.*2870_*2884del, XM_011540370.1:c.*2871_*2884del, XM_011540370.1:c.*2872_*2884del, XM_011540370.1:c.*2873_*2884del, XM_011540370.1:c.*2874_*2884del, XM_011540370.1:c.*2875_*2884del, XM_011540370.1:c.*2876_*2884del, XM_011540370.1:c.*2877_*2884del, XM_011540370.1:c.*2878_*2884del, XM_011540370.1:c.*2879_*2884del, XM_011540370.1:c.*2880_*2884del, XM_011540370.1:c.*2881_*2884del, XM_011540370.1:c.*2882_*2884del, XM_011540370.1:c.*2883_*2884del, XM_011540370.1:c.*2884del, XM_011540370.1:c.*2884dup, XM_011540370.1:c.*2883_*2884dup, XM_011540370.1:c.*2882_*2884dup, XM_011540370.1:c.*2881_*2884dup, XM_011540370.1:c.*2880_*2884dup, XM_011540370.1:c.*2879_*2884dup, XM_011540370.1:c.*2878_*2884dup, XM_011540370.1:c.*2877_*2884dup, XM_011540370.1:c.*2875_*2884dup, XM_011540370.1:c.*2873_*2884dup, XM_011540370.1:c.*2872_*2884dup, XM_011540370.1:c.*2870_*2884dup, XM_011540370.1:c.*2869_*2884dup, XM_011540370.1:c.*2868_*2884dup, XM_011540370.1:c.*2865_*2884dup, XM_011540370.1:c.*2864_*2884dup, XM_011540370.1:c.*2863_*2884dup, XM_011540370.1:c.*2862_*2884dup, XM_011540370.1:c.*2861_*2884dup, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2868_*2884del, XM_047426023.1:c.*2870_*2884del, XM_047426023.1:c.*2871_*2884del, XM_047426023.1:c.*2872_*2884del, XM_047426023.1:c.*2873_*2884del, XM_047426023.1:c.*2874_*2884del, XM_047426023.1:c.*2875_*2884del, XM_047426023.1:c.*2876_*2884del, XM_047426023.1:c.*2877_*2884del, XM_047426023.1:c.*2878_*2884del, XM_047426023.1:c.*2879_*2884del, XM_047426023.1:c.*2880_*2884del, XM_047426023.1:c.*2881_*2884del, XM_047426023.1:c.*2882_*2884del, XM_047426023.1:c.*2883_*2884del, XM_047426023.1:c.*2884del, XM_047426023.1:c.*2884dup, XM_047426023.1:c.*2883_*2884dup, XM_047426023.1:c.*2882_*2884dup, XM_047426023.1:c.*2881_*2884dup, XM_047426023.1:c.*2880_*2884dup, XM_047426023.1:c.*2879_*2884dup, XM_047426023.1:c.*2878_*2884dup, XM_047426023.1:c.*2877_*2884dup, XM_047426023.1:c.*2875_*2884dup, XM_047426023.1:c.*2873_*2884dup, XM_047426023.1:c.*2872_*2884dup, XM_047426023.1:c.*2870_*2884dup, XM_047426023.1:c.*2869_*2884dup, XM_047426023.1:c.*2868_*2884dup, XM_047426023.1:c.*2865_*2884dup, XM_047426023.1:c.*2864_*2884dup, XM_047426023.1:c.*2863_*2884dup, XM_047426023.1:c.*2862_*2884dup, XM_047426023.1:c.*2861_*2884dup, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2868_*2884del, XM_047426026.1:c.*2870_*2884del, XM_047426026.1:c.*2871_*2884del, XM_047426026.1:c.*2872_*2884del, XM_047426026.1:c.*2873_*2884del, XM_047426026.1:c.*2874_*2884del, XM_047426026.1:c.*2875_*2884del, XM_047426026.1:c.*2876_*2884del, XM_047426026.1:c.*2877_*2884del, XM_047426026.1:c.*2878_*2884del, XM_047426026.1:c.*2879_*2884del, XM_047426026.1:c.*2880_*2884del, XM_047426026.1:c.*2881_*2884del, XM_047426026.1:c.*2882_*2884del, XM_047426026.1:c.*2883_*2884del, XM_047426026.1:c.*2884del, XM_047426026.1:c.*2884dup, XM_047426026.1:c.*2883_*2884dup, XM_047426026.1:c.*2882_*2884dup, XM_047426026.1:c.*2881_*2884dup, XM_047426026.1:c.*2880_*2884dup, XM_047426026.1:c.*2879_*2884dup, XM_047426026.1:c.*2878_*2884dup, XM_047426026.1:c.*2877_*2884dup, XM_047426026.1:c.*2875_*2884dup, XM_047426026.1:c.*2873_*2884dup, XM_047426026.1:c.*2872_*2884dup, XM_047426026.1:c.*2870_*2884dup, XM_047426026.1:c.*2869_*2884dup, XM_047426026.1:c.*2868_*2884dup, XM_047426026.1:c.*2865_*2884dup, XM_047426026.1:c.*2864_*2884dup, XM_047426026.1:c.*2863_*2884dup, XM_047426026.1:c.*2862_*2884dup, XM_047426026.1:c.*2861_*2884dup, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2868_*2884del, XM_047426024.1:c.*2870_*2884del, XM_047426024.1:c.*2871_*2884del, XM_047426024.1:c.*2872_*2884del, XM_047426024.1:c.*2873_*2884del, XM_047426024.1:c.*2874_*2884del, XM_047426024.1:c.*2875_*2884del, XM_047426024.1:c.*2876_*2884del, XM_047426024.1:c.*2877_*2884del, XM_047426024.1:c.*2878_*2884del, XM_047426024.1:c.*2879_*2884del, XM_047426024.1:c.*2880_*2884del, XM_047426024.1:c.*2881_*2884del, XM_047426024.1:c.*2882_*2884del, XM_047426024.1:c.*2883_*2884del, XM_047426024.1:c.*2884del, XM_047426024.1:c.*2884dup, XM_047426024.1:c.*2883_*2884dup, XM_047426024.1:c.*2882_*2884dup, XM_047426024.1:c.*2881_*2884dup, XM_047426024.1:c.*2880_*2884dup, XM_047426024.1:c.*2879_*2884dup, XM_047426024.1:c.*2878_*2884dup, XM_047426024.1:c.*2877_*2884dup, XM_047426024.1:c.*2875_*2884dup, XM_047426024.1:c.*2873_*2884dup, XM_047426024.1:c.*2872_*2884dup, XM_047426024.1:c.*2870_*2884dup, XM_047426024.1:c.*2869_*2884dup, XM_047426024.1:c.*2868_*2884dup, XM_047426024.1:c.*2865_*2884dup, XM_047426024.1:c.*2864_*2884dup, XM_047426024.1:c.*2863_*2884dup, XM_047426024.1:c.*2862_*2884dup, XM_047426024.1:c.*2861_*2884dup, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2868_*2884del, XM_047426025.1:c.*2870_*2884del, XM_047426025.1:c.*2871_*2884del, XM_047426025.1:c.*2872_*2884del, XM_047426025.1:c.*2873_*2884del, XM_047426025.1:c.*2874_*2884del, XM_047426025.1:c.*2875_*2884del, XM_047426025.1:c.*2876_*2884del, XM_047426025.1:c.*2877_*2884del, XM_047426025.1:c.*2878_*2884del, XM_047426025.1:c.*2879_*2884del, XM_047426025.1:c.*2880_*2884del, XM_047426025.1:c.*2881_*2884del, XM_047426025.1:c.*2882_*2884del, XM_047426025.1:c.*2883_*2884del, XM_047426025.1:c.*2884del, XM_047426025.1:c.*2884dup, XM_047426025.1:c.*2883_*2884dup, XM_047426025.1:c.*2882_*2884dup, XM_047426025.1:c.*2881_*2884dup, XM_047426025.1:c.*2880_*2884dup, XM_047426025.1:c.*2879_*2884dup, XM_047426025.1:c.*2878_*2884dup, XM_047426025.1:c.*2877_*2884dup, XM_047426025.1:c.*2875_*2884dup, XM_047426025.1:c.*2873_*2884dup, XM_047426025.1:c.*2872_*2884dup, XM_047426025.1:c.*2870_*2884dup, XM_047426025.1:c.*2869_*2884dup, XM_047426025.1:c.*2868_*2884dup, XM_047426025.1:c.*2865_*2884dup, XM_047426025.1:c.*2864_*2884dup, XM_047426025.1:c.*2863_*2884dup, XM_047426025.1:c.*2862_*2884dup, XM_047426025.1:c.*2861_*2884dup, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

        4.

        rs1491483693 has merged into rs1279667652 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
          Chromosome:
          10:96025186 (GRCh38)
          10:97784943 (GRCh37)
          Canonical SPDI:
          NC_000010.11:96025184:AAAAAAAAA:A,NC_000010.11:96025184:AAAAAAAAA:AAA,NC_000010.11:96025184:AAAAAAAAA:AAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:96025184:AAAAAAAAA:AAAAAAAAAAAAAAAA
          Gene:
          CC2D2B (Varview), ENTPD1-AS1 (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,downstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          HGVS:
          NC_000010.11:g.96025186_96025193del, NC_000010.11:g.96025188_96025193del, NC_000010.11:g.96025189_96025193del, NC_000010.11:g.96025190_96025193del, NC_000010.11:g.96025191_96025193del, NC_000010.11:g.96025192_96025193del, NC_000010.11:g.96025193del, NC_000010.11:g.96025193dup, NC_000010.11:g.96025192_96025193dup, NC_000010.11:g.96025191_96025193dup, NC_000010.11:g.96025190_96025193dup, NC_000010.11:g.96025189_96025193dup, NC_000010.11:g.96025187_96025193dup, NC_000010.10:g.97784943_97784950del, NC_000010.10:g.97784945_97784950del, NC_000010.10:g.97784946_97784950del, NC_000010.10:g.97784947_97784950del, NC_000010.10:g.97784948_97784950del, NC_000010.10:g.97784949_97784950del, NC_000010.10:g.97784950del, NC_000010.10:g.97784950dup, NC_000010.10:g.97784949_97784950dup, NC_000010.10:g.97784948_97784950dup, NC_000010.10:g.97784947_97784950dup, NC_000010.10:g.97784946_97784950dup, NC_000010.10:g.97784944_97784950dup

          5.

          rs1491480794 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            AA>- [Show Flanks]
            Chromosome:
            10:96011777 (GRCh38)
            10:97771534 (GRCh37)
            Canonical SPDI:
            NC_000010.11:96011776:AA:
            Gene:
            CC2D2B (Varview), ENTPD1-AS1 (Varview)
            Functional Consequence:
            genic_downstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            -=0./0 (ALFA)
            -=0.03477/134 (ALSPAC)
            -=0.04531/168 (TWINSUK)
            HGVS:

            6.

            rs1491478697 [Homo sapiens]
              Variant type:
              DEL
              Alleles:
              TA>- [Show Flanks]
              Chromosome:
              10:96066946 (GRCh38)
              10:97826703 (GRCh37)
              Canonical SPDI:
              NC_000010.11:96066945:TA:
              Gene:
              ENTPD1-AS1 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              -=0./0 (ALFA)
              -=0.000008/2 (TOPMED)
              HGVS:

              7.

              rs1491465444 [Homo sapiens]
                Variant type:
                INS
                Alleles:
                ->A,AA,AAA [Show Flanks]
                Chromosome:
                10:95762208 (GRCh38)
                10:97521966 (GRCh37)
                Canonical SPDI:
                NC_000010.11:95762208::A,NC_000010.11:95762208::AA,NC_000010.11:95762208::AAA
                Gene:
                ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AA=0./0 (ALFA)
                A=0.000004/1 (TOPMED)
                A=0.000779/13 (TOMMO)
                A=0.00441/8 (Korea1K)
                HGVS:

                8.

                rs1491462166 [Homo sapiens]
                  Variant type:
                  DEL
                  Alleles:
                  CA>- [Show Flanks]
                  Chromosome:
                  10:95754309 (GRCh38)
                  10:97514066 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:95754308:CA:
                  Gene:
                  ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_downstream_transcript_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  -=0.00194/23 (ALFA)
                  HGVS:

                  9.

                  rs1491456540 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ->AT [Show Flanks]
                    Chromosome:
                    10:96024269 (GRCh38)
                    10:97784027 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:96024269:TAT:TATAT
                    Gene:
                    CC2D2B (Varview), ENTPD1-AS1 (Varview)
                    Functional Consequence:
                    genic_downstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    TATAT=0.000084/1 (ALFA)
                    TA=0.000014/2 (GnomAD)
                    HGVS:

                    10.

                    rs1491451536 has merged into rs797010779 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      TT>-,T,TTT,TTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                      Chromosome:
                      10:95979186 (GRCh38)
                      10:97738943 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95979172:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                      Gene:
                      CC2D2B (Varview), ENTPD1-AS1 (Varview)
                      Functional Consequence:
                      genic_upstream_transcript_variant,intron_variant,genic_downstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      TTTTTTTTTTTTTT=0./0 (ALFA)
                      T=0.01/6 (NorthernSweden)
                      HGVS:

                      11.

                      rs1491443122 [Homo sapiens]
                        Variant type:
                        INS
                        Alleles:
                        ->T,TAT,TATAT,TATATAT,TATATATAT,TATATATATAT,TATATATATATAT,TATATATATATATAT,TATATATATATATATAT,TATATATATATATATATAT,TATTTAT [Show Flanks]
                        Chromosome:
                        10:96025185 (GRCh38)
                        10:97784943 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:96025185::T,NC_000010.11:96025185::TAT,NC_000010.11:96025185::TATAT,NC_000010.11:96025185::TATATAT,NC_000010.11:96025185::TATATATAT,NC_000010.11:96025185::TATATATATAT,NC_000010.11:96025185::TATATATATATAT,NC_000010.11:96025185::TATATATATATATAT,NC_000010.11:96025185::TATATATATATATATAT,NC_000010.11:96025185::TATATATATATATATATAT,NC_000010.11:96025185::TATTTAT
                        Gene:
                        CC2D2B (Varview), ENTPD1-AS1 (Varview)
                        Functional Consequence:
                        downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        TAT=0./0 (ALFA)
                        HGVS:
                        NC_000010.11:g.96025185_96025186insT, NC_000010.11:g.96025185_96025186insTAT, NC_000010.11:g.96025185_96025186insTATAT, NC_000010.11:g.96025185_96025186insTATATAT, NC_000010.11:g.96025185_96025186insTATATATAT, NC_000010.11:g.96025185_96025186insTATATATATAT, NC_000010.11:g.96025185_96025186insTATATATATATAT, NC_000010.11:g.96025185_96025186insTATATATATATATAT, NC_000010.11:g.96025185_96025186insTATATATATATATATAT, NC_000010.11:g.96025185_96025186insTATATATATATATATATAT, NC_000010.11:g.96025185_96025186insTATTTAT, NC_000010.10:g.97784942_97784943insT, NC_000010.10:g.97784942_97784943insTAT, NC_000010.10:g.97784942_97784943insTATAT, NC_000010.10:g.97784942_97784943insTATATAT, NC_000010.10:g.97784942_97784943insTATATATAT, NC_000010.10:g.97784942_97784943insTATATATATAT, NC_000010.10:g.97784942_97784943insTATATATATATAT, NC_000010.10:g.97784942_97784943insTATATATATATATAT, NC_000010.10:g.97784942_97784943insTATATATATATATATAT, NC_000010.10:g.97784942_97784943insTATATATATATATATATAT, NC_000010.10:g.97784942_97784943insTATTTAT

                        12.

                        rs1491443071 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          GC>- [Show Flanks]
                          Chromosome:
                          10:95762208 (GRCh38)
                          10:97521965 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:95762207:GC:
                          Gene:
                          ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                          Functional Consequence:
                          genic_downstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0.000449/2 (ALFA)
                          -=0.000183/24 (GnomAD)
                          -=0.000779/13 (TOMMO)
                          HGVS:

                          13.

                          rs1491437168 has merged into rs1555305848 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            CACA>-,CA,CACACA,CACACACA [Show Flanks]
                            Chromosome:
                            10:95856677 (GRCh38)
                            10:97616434 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:95856671:ACACACACA:ACACA,NC_000010.11:95856671:ACACACACA:ACACACA,NC_000010.11:95856671:ACACACACA:ACACACACACA,NC_000010.11:95856671:ACACACACA:ACACACACACACA
                            Gene:
                            ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                            Functional Consequence:
                            genic_downstream_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            ACACACACACA=0./0 (ALFA)
                            AC=0.00042/7 (TOMMO)
                            HGVS:

                            14.

                            rs1491430453 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              CA>- [Show Flanks]
                              Chromosome:
                              10:95934454 (GRCh38)
                              10:97694211 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:95934452:ACA:A
                              Gene:
                              CC2D2B (Varview), ENTPD1-AS1 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by cluster
                              MAF:
                              -=0.000043/6 (GnomAD)
                              -=0.002797/47 (TOMMO)
                              HGVS:

                              15.

                              rs1491427634 has merged into rs1484014389 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TTTT>-,T,TT,TTT,TTTTT [Show Flanks]
                                Chromosome:
                                10:96035132 (GRCh38)
                                10:97794889 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:96035129:TTTTTT:TT,NC_000010.11:96035129:TTTTTT:TTT,NC_000010.11:96035129:TTTTTT:TTTT,NC_000010.11:96035129:TTTTTT:TTTTT,NC_000010.11:96035129:TTTTTT:TTTTTTT
                                Gene:
                                ENTPD1-AS1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TT=0./0 (ALFA)
                                T=0.00007/1 (TOMMO)
                                HGVS:

                                16.

                                rs1491404922 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ->T [Show Flanks]
                                  Chromosome:
                                  10:95847041 (GRCh38)
                                  10:97606799 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:95847041:TTTTTTT:TTTTTTTT
                                  Gene:
                                  ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                  Functional Consequence:
                                  downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  TTTTTTTT=0./0 (ALFA)
                                  T=0.000014/2 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1491386108 [Homo sapiens]
                                    Variant type:
                                    INS
                                    Alleles:
                                    ->A,ATA,ATATA,ATATACATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATATATATATATA,ATATATATATATATATATATATATA,ATATATATATATATATATATATATATA,ATATATG [Show Flanks]
                                    Chromosome:
                                    10:95947114 (GRCh38)
                                    10:97706872 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:95947114::A,NC_000010.11:95947114::ATA,NC_000010.11:95947114::ATATA,NC_000010.11:95947114::ATATACATATA,NC_000010.11:95947114::ATATATA,NC_000010.11:95947114::ATATATATA,NC_000010.11:95947114::ATATATATATA,NC_000010.11:95947114::ATATATATATATA,NC_000010.11:95947114::ATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATATATATATA,NC_000010.11:95947114::ATATATATATATATATATATATATATA,NC_000010.11:95947114::ATATATG
                                    Gene:
                                    CC2D2B (Varview), ENTPD1-AS1 (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    ATA=0./0 (ALFA)
                                    ATATATG=0.000004/1 (TOPMED)
                                    HGVS:
                                    NC_000010.11:g.95947114_95947115insA, NC_000010.11:g.95947114_95947115insATA, NC_000010.11:g.95947114_95947115insATATA, NC_000010.11:g.95947114_95947115insATATACATATA, NC_000010.11:g.95947114_95947115insATATATA, NC_000010.11:g.95947114_95947115insATATATATA, NC_000010.11:g.95947114_95947115insATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATATATATATATATATATATATA, NC_000010.11:g.95947114_95947115insATATATG, NC_000010.10:g.97706871_97706872insA, NC_000010.10:g.97706871_97706872insATA, NC_000010.10:g.97706871_97706872insATATA, NC_000010.10:g.97706871_97706872insATATACATATA, NC_000010.10:g.97706871_97706872insATATATA, NC_000010.10:g.97706871_97706872insATATATATA, NC_000010.10:g.97706871_97706872insATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATATATATATATATATATATATA, NC_000010.10:g.97706871_97706872insATATATG

                                    18.

                                    rs1491380602 [Homo sapiens]
                                      Variant type:
                                      INS
                                      Alleles:
                                      ->T [Show Flanks]
                                      Chromosome:
                                      10:95934453 (GRCh38)
                                      10:97694211 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:95934453::T
                                      Gene:
                                      CC2D2B (Varview), ENTPD1-AS1 (Varview)
                                      Functional Consequence:
                                      genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0.002529/30 (ALFA)
                                      T=0.001996/279 (GnomAD)
                                      T=0.00203/13 (1000Genomes)
                                      HGVS:

                                      19.

                                      rs1491341330 has merged into rs58578983 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
                                        Chromosome:
                                        10:96060638 (GRCh38)
                                        10:97820395 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:96060627:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
                                        Gene:
                                        CCNJ (Varview), ENTPD1-AS1 (Varview)
                                        Functional Consequence:
                                        intron_variant,3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TTTTTTTTTTT=0./0 (ALFA)
                                        T=0.3926/1966 (1000Genomes)
                                        HGVS:
                                        NC_000010.11:g.96060638_96060643del, NC_000010.11:g.96060639_96060643del, NC_000010.11:g.96060640_96060643del, NC_000010.11:g.96060641_96060643del, NC_000010.11:g.96060642_96060643del, NC_000010.11:g.96060643del, NC_000010.11:g.96060643dup, NC_000010.11:g.96060642_96060643dup, NC_000010.11:g.96060641_96060643dup, NC_000010.11:g.96060634_96060643dup, NC_000010.10:g.97820395_97820400del, NC_000010.10:g.97820396_97820400del, NC_000010.10:g.97820397_97820400del, NC_000010.10:g.97820398_97820400del, NC_000010.10:g.97820399_97820400del, NC_000010.10:g.97820400del, NC_000010.10:g.97820400dup, NC_000010.10:g.97820399_97820400dup, NC_000010.10:g.97820398_97820400dup, NC_000010.10:g.97820391_97820400dup, NM_019084.5:c.*2397_*2402del, NM_019084.5:c.*2398_*2402del, NM_019084.5:c.*2399_*2402del, NM_019084.5:c.*2400_*2402del, NM_019084.5:c.*2401_*2402del, NM_019084.5:c.*2402del, NM_019084.5:c.*2402dup, NM_019084.5:c.*2401_*2402dup, NM_019084.5:c.*2400_*2402dup, NM_019084.5:c.*2393_*2402dup, NM_019084.4:c.*2397_*2402del, NM_019084.4:c.*2398_*2402del, NM_019084.4:c.*2399_*2402del, NM_019084.4:c.*2400_*2402del, NM_019084.4:c.*2401_*2402del, NM_019084.4:c.*2402del, NM_019084.4:c.*2402dup, NM_019084.4:c.*2401_*2402dup, NM_019084.4:c.*2400_*2402dup, NM_019084.4:c.*2393_*2402dup, XM_005269921.4:c.*2397_*2402del, XM_005269921.4:c.*2398_*2402del, XM_005269921.4:c.*2399_*2402del, XM_005269921.4:c.*2400_*2402del, XM_005269921.4:c.*2401_*2402del, XM_005269921.4:c.*2402del, XM_005269921.4:c.*2402dup, XM_005269921.4:c.*2401_*2402dup, XM_005269921.4:c.*2400_*2402dup, XM_005269921.4:c.*2393_*2402dup, XM_005269921.2:c.*2397_*2402del, XM_005269921.2:c.*2398_*2402del, XM_005269921.2:c.*2399_*2402del, XM_005269921.2:c.*2400_*2402del, XM_005269921.2:c.*2401_*2402del, XM_005269921.2:c.*2402del, XM_005269921.2:c.*2402dup, XM_005269921.2:c.*2401_*2402dup, XM_005269921.2:c.*2400_*2402dup, XM_005269921.2:c.*2393_*2402dup, XM_005269921.1:c.*2397_*2402del, XM_005269921.1:c.*2398_*2402del, XM_005269921.1:c.*2399_*2402del, XM_005269921.1:c.*2400_*2402del, XM_005269921.1:c.*2401_*2402del, XM_005269921.1:c.*2402del, XM_005269921.1:c.*2402dup, XM_005269921.1:c.*2401_*2402dup, XM_005269921.1:c.*2400_*2402dup, XM_005269921.1:c.*2393_*2402dup, XM_011539885.3:c.*2397_*2402del, XM_011539885.3:c.*2398_*2402del, XM_011539885.3:c.*2399_*2402del, XM_011539885.3:c.*2400_*2402del, XM_011539885.3:c.*2401_*2402del, XM_011539885.3:c.*2402del, XM_011539885.3:c.*2402dup, XM_011539885.3:c.*2401_*2402dup, XM_011539885.3:c.*2400_*2402dup, XM_011539885.3:c.*2393_*2402dup, XM_011539885.1:c.*2397_*2402del, XM_011539885.1:c.*2398_*2402del, XM_011539885.1:c.*2399_*2402del, XM_011539885.1:c.*2400_*2402del, XM_011539885.1:c.*2401_*2402del, XM_011539885.1:c.*2402del, XM_011539885.1:c.*2402dup, XM_011539885.1:c.*2401_*2402dup, XM_011539885.1:c.*2400_*2402dup, XM_011539885.1:c.*2393_*2402dup, XM_017016354.2:c.*2397_*2402del, XM_017016354.2:c.*2398_*2402del, XM_017016354.2:c.*2399_*2402del, XM_017016354.2:c.*2400_*2402del, XM_017016354.2:c.*2401_*2402del, XM_017016354.2:c.*2402del, XM_017016354.2:c.*2402dup, XM_017016354.2:c.*2401_*2402dup, XM_017016354.2:c.*2400_*2402dup, XM_017016354.2:c.*2393_*2402dup, XM_017016354.1:c.*2397_*2402del, XM_017016354.1:c.*2398_*2402del, XM_017016354.1:c.*2399_*2402del, XM_017016354.1:c.*2400_*2402del, XM_017016354.1:c.*2401_*2402del, XM_017016354.1:c.*2402del, XM_017016354.1:c.*2402dup, XM_017016354.1:c.*2401_*2402dup, XM_017016354.1:c.*2400_*2402dup, XM_017016354.1:c.*2393_*2402dup, XM_017016356.2:c.*2397_*2402del, XM_017016356.2:c.*2398_*2402del, XM_017016356.2:c.*2399_*2402del, XM_017016356.2:c.*2400_*2402del, XM_017016356.2:c.*2401_*2402del, XM_017016356.2:c.*2402del, XM_017016356.2:c.*2402dup, XM_017016356.2:c.*2401_*2402dup, XM_017016356.2:c.*2400_*2402dup, XM_017016356.2:c.*2393_*2402dup, XM_017016356.1:c.*2397_*2402del, XM_017016356.1:c.*2398_*2402del, XM_017016356.1:c.*2399_*2402del, XM_017016356.1:c.*2400_*2402del, XM_017016356.1:c.*2401_*2402del, XM_017016356.1:c.*2402del, XM_017016356.1:c.*2402dup, XM_017016356.1:c.*2401_*2402dup, XM_017016356.1:c.*2400_*2402dup, XM_017016356.1:c.*2393_*2402dup, NM_001134375.2:c.*2397_*2402del, NM_001134375.2:c.*2398_*2402del, NM_001134375.2:c.*2399_*2402del, NM_001134375.2:c.*2400_*2402del, NM_001134375.2:c.*2401_*2402del, NM_001134375.2:c.*2402del, NM_001134375.2:c.*2402dup, NM_001134375.2:c.*2401_*2402dup, NM_001134375.2:c.*2400_*2402dup, NM_001134375.2:c.*2393_*2402dup, NM_001134375.1:c.*2397_*2402del, NM_001134375.1:c.*2398_*2402del, NM_001134375.1:c.*2399_*2402del, NM_001134375.1:c.*2400_*2402del, NM_001134375.1:c.*2401_*2402del, NM_001134375.1:c.*2402del, NM_001134375.1:c.*2402dup, NM_001134375.1:c.*2401_*2402dup, NM_001134375.1:c.*2400_*2402dup, NM_001134375.1:c.*2393_*2402dup, NM_001134376.2:c.*2397_*2402del, NM_001134376.2:c.*2398_*2402del, NM_001134376.2:c.*2399_*2402del, NM_001134376.2:c.*2400_*2402del, NM_001134376.2:c.*2401_*2402del, NM_001134376.2:c.*2402del, NM_001134376.2:c.*2402dup, NM_001134376.2:c.*2401_*2402dup, NM_001134376.2:c.*2400_*2402dup, NM_001134376.2:c.*2393_*2402dup, NM_001134376.1:c.*2397_*2402del, NM_001134376.1:c.*2398_*2402del, NM_001134376.1:c.*2399_*2402del, NM_001134376.1:c.*2400_*2402del, NM_001134376.1:c.*2401_*2402del, NM_001134376.1:c.*2402del, NM_001134376.1:c.*2402dup, NM_001134376.1:c.*2401_*2402dup, NM_001134376.1:c.*2400_*2402dup, NM_001134376.1:c.*2393_*2402dup, XM_017016355.2:c.*2397_*2402del, XM_017016355.2:c.*2398_*2402del, XM_017016355.2:c.*2399_*2402del, XM_017016355.2:c.*2400_*2402del, XM_017016355.2:c.*2401_*2402del, XM_017016355.2:c.*2402del, XM_017016355.2:c.*2402dup, XM_017016355.2:c.*2401_*2402dup, XM_017016355.2:c.*2400_*2402dup, XM_017016355.2:c.*2393_*2402dup, XM_017016355.1:c.*2397_*2402del, XM_017016355.1:c.*2398_*2402del, XM_017016355.1:c.*2399_*2402del, XM_017016355.1:c.*2400_*2402del, XM_017016355.1:c.*2401_*2402del, XM_017016355.1:c.*2402del, XM_017016355.1:c.*2402dup, XM_017016355.1:c.*2401_*2402dup, XM_017016355.1:c.*2400_*2402dup, XM_017016355.1:c.*2393_*2402dup, XM_047425381.1:c.*2397_*2402del, XM_047425381.1:c.*2398_*2402del, XM_047425381.1:c.*2399_*2402del, XM_047425381.1:c.*2400_*2402del, XM_047425381.1:c.*2401_*2402del, XM_047425381.1:c.*2402del, XM_047425381.1:c.*2402dup, XM_047425381.1:c.*2401_*2402dup, XM_047425381.1:c.*2400_*2402dup, XM_047425381.1:c.*2393_*2402dup

                                        20.

                                        rs1491319715 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          ->A [Show Flanks]
                                          Chromosome:
                                          10:96066946 (GRCh38)
                                          10:97826704 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:96066946:AAAA:AAAAA
                                          Gene:
                                          ENTPD1-AS1 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          AAAAA=0./0 (ALFA)
                                          A=0.0001/14 (GnomAD)
                                          A=0.000132/35 (TOPMED)
                                          A=0.000389/7 (TOMMO)
                                          HGVS:

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