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1.

rs1491547500 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->ACAAA [Show Flanks]
    Chromosome:
    5:126798134 (GRCh38)
    5:126133827 (GRCh37)
    Canonical SPDI:
    NC_000005.10:126798134:AAA:AAAACAAA
    Gene:
    LMNB1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    AAAACAAA=0./0 (ALFA)
    AAAAC=0.000015/2 (GnomAD)
    HGVS:

    2.

    rs1491545510 has merged into rs34534973 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTTTTTTTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      5:126796796 (GRCh38)
      5:126132488 (GRCh37)
      Canonical SPDI:
      NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126796786:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      LMNB1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTTTTT=0./0 (ALFA)
      -=0.000019/5 (TOPMED)
      HGVS:
      NC_000005.10:g.126796796_126796806del, NC_000005.10:g.126796797_126796806del, NC_000005.10:g.126796798_126796806del, NC_000005.10:g.126796799_126796806del, NC_000005.10:g.126796801_126796806del, NC_000005.10:g.126796802_126796806del, NC_000005.10:g.126796803_126796806del, NC_000005.10:g.126796804_126796806del, NC_000005.10:g.126796805_126796806del, NC_000005.10:g.126796806del, NC_000005.10:g.126796806dup, NC_000005.10:g.126796805_126796806dup, NC_000005.10:g.126796804_126796806dup, NC_000005.10:g.126796803_126796806dup, NC_000005.10:g.126796802_126796806dup, NC_000005.10:g.126796787_126796806T[25]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.10:g.126796787_126796806T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.10:g.126796801_126796806dup, NC_000005.10:g.126796800_126796806dup, NC_000005.10:g.126796799_126796806dup, NC_000005.10:g.126796798_126796806dup, NC_000005.10:g.126796797_126796806dup, NC_000005.10:g.126796796_126796806dup, NC_000005.10:g.126796795_126796806dup, NC_000005.10:g.126796794_126796806dup, NC_000005.10:g.126796793_126796806dup, NC_000005.10:g.126796792_126796806dup, NC_000005.10:g.126796791_126796806dup, NC_000005.10:g.126796790_126796806dup, NC_000005.10:g.126796789_126796806dup, NC_000005.10:g.126796788_126796806dup, NC_000005.10:g.126796787_126796806dup, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796787_126796806T[44]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126796806_126796807insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132488_126132498del, NC_000005.9:g.126132489_126132498del, NC_000005.9:g.126132490_126132498del, NC_000005.9:g.126132491_126132498del, NC_000005.9:g.126132493_126132498del, NC_000005.9:g.126132494_126132498del, NC_000005.9:g.126132495_126132498del, NC_000005.9:g.126132496_126132498del, NC_000005.9:g.126132497_126132498del, NC_000005.9:g.126132498del, NC_000005.9:g.126132498dup, NC_000005.9:g.126132497_126132498dup, NC_000005.9:g.126132496_126132498dup, NC_000005.9:g.126132495_126132498dup, NC_000005.9:g.126132494_126132498dup, NC_000005.9:g.126132479_126132498T[25]CTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.9:g.126132479_126132498T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.9:g.126132493_126132498dup, NC_000005.9:g.126132492_126132498dup, NC_000005.9:g.126132491_126132498dup, NC_000005.9:g.126132490_126132498dup, NC_000005.9:g.126132489_126132498dup, NC_000005.9:g.126132488_126132498dup, NC_000005.9:g.126132487_126132498dup, NC_000005.9:g.126132486_126132498dup, NC_000005.9:g.126132485_126132498dup, NC_000005.9:g.126132484_126132498dup, NC_000005.9:g.126132483_126132498dup, NC_000005.9:g.126132482_126132498dup, NC_000005.9:g.126132481_126132498dup, NC_000005.9:g.126132480_126132498dup, NC_000005.9:g.126132479_126132498dup, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132479_126132498T[44]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126132498_126132499insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24656_24666del, NG_008360.2:g.24657_24666del, NG_008360.2:g.24658_24666del, NG_008360.2:g.24659_24666del, NG_008360.2:g.24661_24666del, NG_008360.2:g.24662_24666del, NG_008360.2:g.24663_24666del, NG_008360.2:g.24664_24666del, NG_008360.2:g.24665_24666del, NG_008360.2:g.24666del, NG_008360.2:g.24666dup, NG_008360.2:g.24665_24666dup, NG_008360.2:g.24664_24666dup, NG_008360.2:g.24663_24666dup, NG_008360.2:g.24662_24666dup, NG_008360.2:g.24647_24666T[25]CTTTTTTTTTTTTTTTTTTTTT[1], NG_008360.2:g.24647_24666T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008360.2:g.24661_24666dup, NG_008360.2:g.24660_24666dup, NG_008360.2:g.24659_24666dup, NG_008360.2:g.24658_24666dup, NG_008360.2:g.24657_24666dup, NG_008360.2:g.24656_24666dup, NG_008360.2:g.24655_24666dup, NG_008360.2:g.24654_24666dup, NG_008360.2:g.24653_24666dup, NG_008360.2:g.24652_24666dup, NG_008360.2:g.24651_24666dup, NG_008360.2:g.24650_24666dup, NG_008360.2:g.24649_24666dup, NG_008360.2:g.24648_24666dup, NG_008360.2:g.24647_24666dup, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24647_24666T[44]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.24666_24667insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

      3.

      rs1491525523 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        AT>- [Show Flanks]
        Chromosome:
        5:126784014 (GRCh38)
        5:126119706 (GRCh37)
        Canonical SPDI:
        NC_000005.10:126784013:AT:
        Gene:
        LMNB1 (Varview)
        Functional Consequence:
        genic_upstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0./0 (ALFA)
        HGVS:

        4.

        rs1491469893 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->CTTTT [Show Flanks]
          Chromosome:
          5:126837357 (GRCh38)
          5:126173050 (GRCh37)
          Canonical SPDI:
          NC_000005.10:126837357:TTTT:TTTTCTTTT
          Gene:
          LMNB1 (Varview)
          Functional Consequence:
          500B_downstream_variant,downstream_transcript_variant
          Validated:
          by frequency,by alfa
          MAF:
          TTTTCTTTT=0.00008/1 (ALFA)
          HGVS:

          5.

          rs1491462732 [Homo sapiens]
            Variant type:
            SNV:
            Alleles:
            ->TTTTTTTTTCTTTTTTTTTTTTTTTTT
            Chromosome:
            no mapping
            Canonical SPDI:

            6.

            rs1491448646 has merged into rs61578729 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              5:126784025 (GRCh38)
              5:126119717 (GRCh37)
              Canonical SPDI:
              NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126784014:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              LMNB1 (Varview)
              Functional Consequence:
              intron_variant,genic_upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTTTT=0./0 (ALFA)
              -=0.425/17 (GENOME_DK)
              HGVS:
              NC_000005.10:g.126784025_126784041del, NC_000005.10:g.126784026_126784041del, NC_000005.10:g.126784027_126784041del, NC_000005.10:g.126784028_126784041del, NC_000005.10:g.126784029_126784041del, NC_000005.10:g.126784030_126784041del, NC_000005.10:g.126784031_126784041del, NC_000005.10:g.126784032_126784041del, NC_000005.10:g.126784033_126784041del, NC_000005.10:g.126784034_126784041del, NC_000005.10:g.126784035_126784041del, NC_000005.10:g.126784036_126784041del, NC_000005.10:g.126784037_126784041del, NC_000005.10:g.126784038_126784041del, NC_000005.10:g.126784039_126784041del, NC_000005.10:g.126784040_126784041del, NC_000005.10:g.126784041del, NC_000005.10:g.126784041dup, NC_000005.10:g.126784040_126784041dup, NC_000005.10:g.126784039_126784041dup, NC_000005.10:g.126784038_126784041dup, NC_000005.10:g.126784037_126784041dup, NC_000005.10:g.126784035_126784041dup, NC_000005.10:g.126784034_126784041dup, NC_000005.10:g.126784024_126784041dup, NC_000005.10:g.126784016_126784041dup, NC_000005.10:g.126784041_126784042insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126784041_126784042insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126119717_126119733del, NC_000005.9:g.126119718_126119733del, NC_000005.9:g.126119719_126119733del, NC_000005.9:g.126119720_126119733del, NC_000005.9:g.126119721_126119733del, NC_000005.9:g.126119722_126119733del, NC_000005.9:g.126119723_126119733del, NC_000005.9:g.126119724_126119733del, NC_000005.9:g.126119725_126119733del, NC_000005.9:g.126119726_126119733del, NC_000005.9:g.126119727_126119733del, NC_000005.9:g.126119728_126119733del, NC_000005.9:g.126119729_126119733del, NC_000005.9:g.126119730_126119733del, NC_000005.9:g.126119731_126119733del, NC_000005.9:g.126119732_126119733del, NC_000005.9:g.126119733del, NC_000005.9:g.126119733dup, NC_000005.9:g.126119732_126119733dup, NC_000005.9:g.126119731_126119733dup, NC_000005.9:g.126119730_126119733dup, NC_000005.9:g.126119729_126119733dup, NC_000005.9:g.126119727_126119733dup, NC_000005.9:g.126119726_126119733dup, NC_000005.9:g.126119716_126119733dup, NC_000005.9:g.126119708_126119733dup, NC_000005.9:g.126119733_126119734insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126119733_126119734insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.11885_11901del, NG_008360.2:g.11886_11901del, NG_008360.2:g.11887_11901del, NG_008360.2:g.11888_11901del, NG_008360.2:g.11889_11901del, NG_008360.2:g.11890_11901del, NG_008360.2:g.11891_11901del, NG_008360.2:g.11892_11901del, NG_008360.2:g.11893_11901del, NG_008360.2:g.11894_11901del, NG_008360.2:g.11895_11901del, NG_008360.2:g.11896_11901del, NG_008360.2:g.11897_11901del, NG_008360.2:g.11898_11901del, NG_008360.2:g.11899_11901del, NG_008360.2:g.11900_11901del, NG_008360.2:g.11901del, NG_008360.2:g.11901dup, NG_008360.2:g.11900_11901dup, NG_008360.2:g.11899_11901dup, NG_008360.2:g.11898_11901dup, NG_008360.2:g.11897_11901dup, NG_008360.2:g.11895_11901dup, NG_008360.2:g.11894_11901dup, NG_008360.2:g.11884_11901dup, NG_008360.2:g.11876_11901dup, NG_008360.2:g.11901_11902insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.11901_11902insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

              7.

              rs1491373758 has merged into rs149759920 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                GAGAGAGAGA>-,GAGA,GAGAGA,GAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGA [Show Flanks]
                Chromosome:
                5:126806610 (GRCh38)
                5:126142302 (GRCh37)
                Canonical SPDI:
                NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGA,NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGAGAGA,NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGAGAGAGA,NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA,NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA,NC_000005.10:126806602:AGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA
                Gene:
                LMNB1 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AGAGAGAGAGA=0./0 (ALFA)
                AG=0.00004/1 (TOMMO)
                AG=0.00156/7 (Estonian)
                HGVS:

                8.

                rs1491327123 has merged into rs142332901 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  5:126787559 (GRCh38)
                  5:126123251 (GRCh37)
                  Canonical SPDI:
                  NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126787546:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  LMNB1 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTTTTTT=0./0 (ALFA)
                  -=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000005.10:g.126787559_126787564del, NC_000005.10:g.126787560_126787564del, NC_000005.10:g.126787561_126787564del, NC_000005.10:g.126787562_126787564del, NC_000005.10:g.126787563_126787564del, NC_000005.10:g.126787564del, NC_000005.10:g.126787564dup, NC_000005.10:g.126787563_126787564dup, NC_000005.10:g.126787562_126787564dup, NC_000005.10:g.126787561_126787564dup, NC_000005.10:g.126787560_126787564dup, NC_000005.10:g.126787559_126787564dup, NC_000005.10:g.126787558_126787564dup, NC_000005.10:g.126787557_126787564dup, NC_000005.10:g.126787556_126787564dup, NC_000005.10:g.126787555_126787564dup, NC_000005.10:g.126787554_126787564dup, NC_000005.10:g.126787553_126787564dup, NC_000005.10:g.126787552_126787564dup, NC_000005.10:g.126787551_126787564dup, NC_000005.10:g.126787550_126787564dup, NC_000005.10:g.126787549_126787564dup, NC_000005.10:g.126787548_126787564dup, NC_000005.10:g.126787547_126787564dup, NC_000005.10:g.126787564_126787565insTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126787564_126787565insTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126787564_126787565insTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126787564_126787565insTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126787564_126787565insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126123251_126123256del, NC_000005.9:g.126123252_126123256del, NC_000005.9:g.126123253_126123256del, NC_000005.9:g.126123254_126123256del, NC_000005.9:g.126123255_126123256del, NC_000005.9:g.126123256del, NC_000005.9:g.126123256dup, NC_000005.9:g.126123255_126123256dup, NC_000005.9:g.126123254_126123256dup, NC_000005.9:g.126123253_126123256dup, NC_000005.9:g.126123252_126123256dup, NC_000005.9:g.126123251_126123256dup, NC_000005.9:g.126123250_126123256dup, NC_000005.9:g.126123249_126123256dup, NC_000005.9:g.126123248_126123256dup, NC_000005.9:g.126123247_126123256dup, NC_000005.9:g.126123246_126123256dup, NC_000005.9:g.126123245_126123256dup, NC_000005.9:g.126123244_126123256dup, NC_000005.9:g.126123243_126123256dup, NC_000005.9:g.126123242_126123256dup, NC_000005.9:g.126123241_126123256dup, NC_000005.9:g.126123240_126123256dup, NC_000005.9:g.126123239_126123256dup, NC_000005.9:g.126123256_126123257insTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126123256_126123257insTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126123256_126123257insTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126123256_126123257insTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126123256_126123257insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.15419_15424del, NG_008360.2:g.15420_15424del, NG_008360.2:g.15421_15424del, NG_008360.2:g.15422_15424del, NG_008360.2:g.15423_15424del, NG_008360.2:g.15424del, NG_008360.2:g.15424dup, NG_008360.2:g.15423_15424dup, NG_008360.2:g.15422_15424dup, NG_008360.2:g.15421_15424dup, NG_008360.2:g.15420_15424dup, NG_008360.2:g.15419_15424dup, NG_008360.2:g.15418_15424dup, NG_008360.2:g.15417_15424dup, NG_008360.2:g.15416_15424dup, NG_008360.2:g.15415_15424dup, NG_008360.2:g.15414_15424dup, NG_008360.2:g.15413_15424dup, NG_008360.2:g.15412_15424dup, NG_008360.2:g.15411_15424dup, NG_008360.2:g.15410_15424dup, NG_008360.2:g.15409_15424dup, NG_008360.2:g.15408_15424dup, NG_008360.2:g.15407_15424dup, NG_008360.2:g.15424_15425insTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.15424_15425insTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.15424_15425insTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.15424_15425insTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.15424_15425insTTTTTTTTTTTTTTTTTTTTTTTTT

                  9.

                  rs1491321860 [Homo sapiens]
                    Variant type:
                    DEL
                    Alleles:
                    AT>- [Show Flanks]
                    Chromosome:
                    5:126785295 (GRCh38)
                    5:126120987 (GRCh37)
                    Canonical SPDI:
                    NC_000005.10:126785294:AT:
                    Gene:
                    LMNB1 (Varview)
                    Functional Consequence:
                    genic_upstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    -=0.000084/1 (ALFA)
                    -=0.000041/5 (GnomAD)
                    HGVS:

                    10.

                    rs1491295772 has merged into rs35987371 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      TT>-,T,TTT [Show Flanks]
                      Chromosome:
                      5:126788916 (GRCh38)
                      5:126124608 (GRCh37)
                      Canonical SPDI:
                      NC_000005.10:126788905:TTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:126788905:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:126788905:TTTTTTTTTTTT:TTTTTTTTTTTTT
                      Gene:
                      LMNB1 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      TTTTTTTTTTTTT=0.001/6 (ALFA)
                      T=0.25/10 (GENOME_DK)
                      T=0.3438/1722 (1000Genomes)
                      HGVS:

                      11.

                      rs1491279848 has merged into rs57113826 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        TATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
                        Chromosome:
                        5:126800964 (GRCh38)
                        5:126136656 (GRCh37)
                        Canonical SPDI:
                        NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000005.10:126800951:TATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA
                        Gene:
                        LMNB1 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        TATATATATATA=0./0 (ALFA)
                        HGVS:
                        NC_000005.10:g.126800952TA[6], NC_000005.10:g.126800952TA[7], NC_000005.10:g.126800952TA[8], NC_000005.10:g.126800952TA[9], NC_000005.10:g.126800952TA[10], NC_000005.10:g.126800952TA[11], NC_000005.10:g.126800952TA[12], NC_000005.10:g.126800952TA[13], NC_000005.10:g.126800952TA[14], NC_000005.10:g.126800952TA[16], NC_000005.10:g.126800952TA[17], NC_000005.10:g.126800952TA[18], NC_000005.10:g.126800952TA[19], NC_000005.10:g.126800952TA[20], NC_000005.10:g.126800952TA[21], NC_000005.10:g.126800952TA[22], NC_000005.10:g.126800952TA[23], NC_000005.10:g.126800952TA[24], NC_000005.10:g.126800952TA[25], NC_000005.10:g.126800952TA[26], NC_000005.10:g.126800952TA[27], NC_000005.10:g.126800952TA[28], NC_000005.9:g.126136644TA[6], NC_000005.9:g.126136644TA[7], NC_000005.9:g.126136644TA[8], NC_000005.9:g.126136644TA[9], NC_000005.9:g.126136644TA[10], NC_000005.9:g.126136644TA[11], NC_000005.9:g.126136644TA[12], NC_000005.9:g.126136644TA[13], NC_000005.9:g.126136644TA[14], NC_000005.9:g.126136644TA[16], NC_000005.9:g.126136644TA[17], NC_000005.9:g.126136644TA[18], NC_000005.9:g.126136644TA[19], NC_000005.9:g.126136644TA[20], NC_000005.9:g.126136644TA[21], NC_000005.9:g.126136644TA[22], NC_000005.9:g.126136644TA[23], NC_000005.9:g.126136644TA[24], NC_000005.9:g.126136644TA[25], NC_000005.9:g.126136644TA[26], NC_000005.9:g.126136644TA[27], NC_000005.9:g.126136644TA[28], NG_008360.2:g.28812TA[6], NG_008360.2:g.28812TA[7], NG_008360.2:g.28812TA[8], NG_008360.2:g.28812TA[9], NG_008360.2:g.28812TA[10], NG_008360.2:g.28812TA[11], NG_008360.2:g.28812TA[12], NG_008360.2:g.28812TA[13], NG_008360.2:g.28812TA[14], NG_008360.2:g.28812TA[16], NG_008360.2:g.28812TA[17], NG_008360.2:g.28812TA[18], NG_008360.2:g.28812TA[19], NG_008360.2:g.28812TA[20], NG_008360.2:g.28812TA[21], NG_008360.2:g.28812TA[22], NG_008360.2:g.28812TA[23], NG_008360.2:g.28812TA[24], NG_008360.2:g.28812TA[25], NG_008360.2:g.28812TA[26], NG_008360.2:g.28812TA[27], NG_008360.2:g.28812TA[28]

                        12.

                        rs1491276839 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          AA>- [Show Flanks]
                          Chromosome:
                          5:126800981 (GRCh38)
                          5:126136673 (GRCh37)
                          Canonical SPDI:
                          NC_000005.10:126800980:AA:
                          Gene:
                          LMNB1 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0./0 (ALFA)
                          -=0.05241/3285 (GnomAD)
                          -=0.07688/127 (Korea1K)
                          -=0.07862/1233 (TOMMO)
                          HGVS:

                          13.

                          rs1491264660 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            ->GCTTTACAGACATTATCTTTTTTTT [Show Flanks]
                            Chromosome:
                            5:126786113 (GRCh38)
                            5:126121806 (GRCh37)
                            Canonical SPDI:
                            NC_000005.10:126786113:TTTTTTTT:TTTTTTTTGCTTTACAGACATTATCTTTTTTTT
                            Gene:
                            LMNB1 (Varview)
                            Functional Consequence:
                            genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTTTTTGCTTTACAGACATTATCTTTTTTTT=0.00017/2 (ALFA)
                            TTTTTTTTGCTTTACAGACATTATC=0.01975/292 (GnomAD)
                            HGVS:

                            14.

                            rs1491197725 has merged into rs563852961 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                              Chromosome:
                              5:126837368 (GRCh38)
                              5:126173060 (GRCh37)
                              Canonical SPDI:
                              NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126837356:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                              Gene:
                              LMNB1 (Varview)
                              Functional Consequence:
                              500B_downstream_variant,downstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TTTTTTTTTTTT=0./0 (ALFA)
                              HGVS:
                              NC_000005.10:g.126837368_126837377del, NC_000005.10:g.126837369_126837377del, NC_000005.10:g.126837370_126837377del, NC_000005.10:g.126837371_126837377del, NC_000005.10:g.126837372_126837377del, NC_000005.10:g.126837373_126837377del, NC_000005.10:g.126837374_126837377del, NC_000005.10:g.126837375_126837377del, NC_000005.10:g.126837376_126837377del, NC_000005.10:g.126837377del, NC_000005.10:g.126837377dup, NC_000005.10:g.126837376_126837377dup, NC_000005.10:g.126837375_126837377dup, NC_000005.10:g.126837374_126837377dup, NC_000005.10:g.126837373_126837377dup, NC_000005.10:g.126837372_126837377dup, NC_000005.10:g.126837371_126837377dup, NC_000005.10:g.126837370_126837377dup, NC_000005.10:g.126837369_126837377dup, NC_000005.10:g.126837368_126837377dup, NC_000005.10:g.126837367_126837377dup, NC_000005.10:g.126837366_126837377dup, NC_000005.10:g.126837365_126837377dup, NC_000005.10:g.126837364_126837377dup, NC_000005.10:g.126837363_126837377dup, NC_000005.10:g.126837361_126837377dup, NC_000005.9:g.126173060_126173069del, NC_000005.9:g.126173061_126173069del, NC_000005.9:g.126173062_126173069del, NC_000005.9:g.126173063_126173069del, NC_000005.9:g.126173064_126173069del, NC_000005.9:g.126173065_126173069del, NC_000005.9:g.126173066_126173069del, NC_000005.9:g.126173067_126173069del, NC_000005.9:g.126173068_126173069del, NC_000005.9:g.126173069del, NC_000005.9:g.126173069dup, NC_000005.9:g.126173068_126173069dup, NC_000005.9:g.126173067_126173069dup, NC_000005.9:g.126173066_126173069dup, NC_000005.9:g.126173065_126173069dup, NC_000005.9:g.126173064_126173069dup, NC_000005.9:g.126173063_126173069dup, NC_000005.9:g.126173062_126173069dup, NC_000005.9:g.126173061_126173069dup, NC_000005.9:g.126173060_126173069dup, NC_000005.9:g.126173059_126173069dup, NC_000005.9:g.126173058_126173069dup, NC_000005.9:g.126173057_126173069dup, NC_000005.9:g.126173056_126173069dup, NC_000005.9:g.126173055_126173069dup, NC_000005.9:g.126173053_126173069dup, NG_008360.2:g.65228_65237del, NG_008360.2:g.65229_65237del, NG_008360.2:g.65230_65237del, NG_008360.2:g.65231_65237del, NG_008360.2:g.65232_65237del, NG_008360.2:g.65233_65237del, NG_008360.2:g.65234_65237del, NG_008360.2:g.65235_65237del, NG_008360.2:g.65236_65237del, NG_008360.2:g.65237del, NG_008360.2:g.65237dup, NG_008360.2:g.65236_65237dup, NG_008360.2:g.65235_65237dup, NG_008360.2:g.65234_65237dup, NG_008360.2:g.65233_65237dup, NG_008360.2:g.65232_65237dup, NG_008360.2:g.65231_65237dup, NG_008360.2:g.65230_65237dup, NG_008360.2:g.65229_65237dup, NG_008360.2:g.65228_65237dup, NG_008360.2:g.65227_65237dup, NG_008360.2:g.65226_65237dup, NG_008360.2:g.65225_65237dup, NG_008360.2:g.65224_65237dup, NG_008360.2:g.65223_65237dup, NG_008360.2:g.65221_65237dup

                              15.

                              rs1491166596 has merged into rs869071732 [Homo sapiens]
                                Variant type:
                                INS
                                Alleles:
                                ->A,AC,ACA,ATA,ATATA,ATATACA,ATATATA,ATATATACA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATATATATATATA,ATATATTTA,ATGTA [Show Flanks]
                                Chromosome:
                                5:126787547 (GRCh38)
                                5:126123240 (GRCh37)
                                Canonical SPDI:
                                NC_000005.10:126787547::A,NC_000005.10:126787547::AC,NC_000005.10:126787547::ACA,NC_000005.10:126787547::ATA,NC_000005.10:126787547::ATATA,NC_000005.10:126787547::ATATACA,NC_000005.10:126787547::ATATATA,NC_000005.10:126787547::ATATATACA,NC_000005.10:126787547::ATATATATA,NC_000005.10:126787547::ATATATATATA,NC_000005.10:126787547::ATATATATATATA,NC_000005.10:126787547::ATATATATATATATA,NC_000005.10:126787547::ATATATATATATATATA,NC_000005.10:126787547::ATATATATATATATATATA,NC_000005.10:126787547::ATATATATATATATATATATA,NC_000005.10:126787547::ATATATATATATATATATATATA,NC_000005.10:126787547::ATATATTTA,NC_000005.10:126787547::ATGTA
                                Gene:
                                LMNB1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                ACA=0./0 (ALFA)
                                A=0.0487/22 (NorthernSweden)
                                HGVS:
                                NC_000005.10:g.126787547_126787548insA, NC_000005.10:g.126787547_126787548insAC, NC_000005.10:g.126787547_126787548insACA, NC_000005.10:g.126787547_126787548insATA, NC_000005.10:g.126787547_126787548insATATA, NC_000005.10:g.126787547_126787548insATATACA, NC_000005.10:g.126787547_126787548insATATATA, NC_000005.10:g.126787547_126787548insATATATACA, NC_000005.10:g.126787547_126787548insATATATATA, NC_000005.10:g.126787547_126787548insATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATATATATATA, NC_000005.10:g.126787547_126787548insATATATATATATATATATATATA, NC_000005.10:g.126787547_126787548insATATATTTA, NC_000005.10:g.126787547_126787548insATGTA, NC_000005.9:g.126123239_126123240insA, NC_000005.9:g.126123239_126123240insAC, NC_000005.9:g.126123239_126123240insACA, NC_000005.9:g.126123239_126123240insATA, NC_000005.9:g.126123239_126123240insATATA, NC_000005.9:g.126123239_126123240insATATACA, NC_000005.9:g.126123239_126123240insATATATA, NC_000005.9:g.126123239_126123240insATATATACA, NC_000005.9:g.126123239_126123240insATATATATA, NC_000005.9:g.126123239_126123240insATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATATATATATA, NC_000005.9:g.126123239_126123240insATATATATATATATATATATATA, NC_000005.9:g.126123239_126123240insATATATTTA, NC_000005.9:g.126123239_126123240insATGTA, NG_008360.2:g.15407_15408insA, NG_008360.2:g.15407_15408insAC, NG_008360.2:g.15407_15408insACA, NG_008360.2:g.15407_15408insATA, NG_008360.2:g.15407_15408insATATA, NG_008360.2:g.15407_15408insATATACA, NG_008360.2:g.15407_15408insATATATA, NG_008360.2:g.15407_15408insATATATACA, NG_008360.2:g.15407_15408insATATATATA, NG_008360.2:g.15407_15408insATATATATATA, NG_008360.2:g.15407_15408insATATATATATATA, NG_008360.2:g.15407_15408insATATATATATATATA, NG_008360.2:g.15407_15408insATATATATATATATATA, NG_008360.2:g.15407_15408insATATATATATATATATATA, NG_008360.2:g.15407_15408insATATATATATATATATATATA, NG_008360.2:g.15407_15408insATATATATATATATATATATATA, NG_008360.2:g.15407_15408insATATATTTA, NG_008360.2:g.15407_15408insATGTA

                                16.

                                rs1491101365 [Homo sapiens]
                                  Variant type:
                                  SNV:
                                  Alleles:
                                  ->TTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT
                                  Chromosome:
                                  no mapping
                                  Canonical SPDI:

                                  17.

                                  rs1491038520 has merged into rs11430160 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                    Chromosome:
                                    5:126812727 (GRCh38)
                                    5:126148419 (GRCh37)
                                    Canonical SPDI:
                                    NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:126812718:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                    Gene:
                                    LMNB1 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    TTTTTTTT=0./0 (ALFA)
                                    -=0.000004/1 (TOPMED)
                                    -=0.452476/2266 (1000Genomes)
                                    HGVS:
                                    NC_000005.10:g.126812727_126812742del, NC_000005.10:g.126812728_126812742del, NC_000005.10:g.126812729_126812742del, NC_000005.10:g.126812730_126812742del, NC_000005.10:g.126812731_126812742del, NC_000005.10:g.126812732_126812742del, NC_000005.10:g.126812733_126812742del, NC_000005.10:g.126812734_126812742del, NC_000005.10:g.126812735_126812742del, NC_000005.10:g.126812736_126812742del, NC_000005.10:g.126812737_126812742del, NC_000005.10:g.126812738_126812742del, NC_000005.10:g.126812740_126812742del, NC_000005.10:g.126812741_126812742del, NC_000005.10:g.126812742del, NC_000005.10:g.126812742dup, NC_000005.10:g.126812741_126812742dup, NC_000005.10:g.126812740_126812742dup, NC_000005.10:g.126812739_126812742dup, NC_000005.10:g.126812738_126812742dup, NC_000005.10:g.126812737_126812742dup, NC_000005.10:g.126812736_126812742dup, NC_000005.10:g.126812735_126812742dup, NC_000005.10:g.126812734_126812742dup, NC_000005.10:g.126812733_126812742dup, NC_000005.10:g.126812732_126812742dup, NC_000005.10:g.126812731_126812742dup, NC_000005.10:g.126812730_126812742dup, NC_000005.10:g.126812729_126812742dup, NC_000005.10:g.126812728_126812742dup, NC_000005.10:g.126812727_126812742dup, NC_000005.10:g.126812726_126812742dup, NC_000005.10:g.126812725_126812742dup, NC_000005.10:g.126812724_126812742dup, NC_000005.10:g.126812723_126812742dup, NC_000005.10:g.126812722_126812742dup, NC_000005.10:g.126812721_126812742dup, NC_000005.10:g.126812720_126812742dup, NC_000005.10:g.126812742_126812743insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.126812742_126812743insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126148419_126148434del, NC_000005.9:g.126148420_126148434del, NC_000005.9:g.126148421_126148434del, NC_000005.9:g.126148422_126148434del, NC_000005.9:g.126148423_126148434del, NC_000005.9:g.126148424_126148434del, NC_000005.9:g.126148425_126148434del, NC_000005.9:g.126148426_126148434del, NC_000005.9:g.126148427_126148434del, NC_000005.9:g.126148428_126148434del, NC_000005.9:g.126148429_126148434del, NC_000005.9:g.126148430_126148434del, NC_000005.9:g.126148432_126148434del, NC_000005.9:g.126148433_126148434del, NC_000005.9:g.126148434del, NC_000005.9:g.126148434dup, NC_000005.9:g.126148433_126148434dup, NC_000005.9:g.126148432_126148434dup, NC_000005.9:g.126148431_126148434dup, NC_000005.9:g.126148430_126148434dup, NC_000005.9:g.126148429_126148434dup, NC_000005.9:g.126148428_126148434dup, NC_000005.9:g.126148427_126148434dup, NC_000005.9:g.126148426_126148434dup, NC_000005.9:g.126148425_126148434dup, NC_000005.9:g.126148424_126148434dup, NC_000005.9:g.126148423_126148434dup, NC_000005.9:g.126148422_126148434dup, NC_000005.9:g.126148421_126148434dup, NC_000005.9:g.126148420_126148434dup, NC_000005.9:g.126148419_126148434dup, NC_000005.9:g.126148418_126148434dup, NC_000005.9:g.126148417_126148434dup, NC_000005.9:g.126148416_126148434dup, NC_000005.9:g.126148415_126148434dup, NC_000005.9:g.126148414_126148434dup, NC_000005.9:g.126148413_126148434dup, NC_000005.9:g.126148412_126148434dup, NC_000005.9:g.126148434_126148435insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.126148434_126148435insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.40587_40602del, NG_008360.2:g.40588_40602del, NG_008360.2:g.40589_40602del, NG_008360.2:g.40590_40602del, NG_008360.2:g.40591_40602del, NG_008360.2:g.40592_40602del, NG_008360.2:g.40593_40602del, NG_008360.2:g.40594_40602del, NG_008360.2:g.40595_40602del, NG_008360.2:g.40596_40602del, NG_008360.2:g.40597_40602del, NG_008360.2:g.40598_40602del, NG_008360.2:g.40600_40602del, NG_008360.2:g.40601_40602del, NG_008360.2:g.40602del, NG_008360.2:g.40602dup, NG_008360.2:g.40601_40602dup, NG_008360.2:g.40600_40602dup, NG_008360.2:g.40599_40602dup, NG_008360.2:g.40598_40602dup, NG_008360.2:g.40597_40602dup, NG_008360.2:g.40596_40602dup, NG_008360.2:g.40595_40602dup, NG_008360.2:g.40594_40602dup, NG_008360.2:g.40593_40602dup, NG_008360.2:g.40592_40602dup, NG_008360.2:g.40591_40602dup, NG_008360.2:g.40590_40602dup, NG_008360.2:g.40589_40602dup, NG_008360.2:g.40588_40602dup, NG_008360.2:g.40587_40602dup, NG_008360.2:g.40586_40602dup, NG_008360.2:g.40585_40602dup, NG_008360.2:g.40584_40602dup, NG_008360.2:g.40583_40602dup, NG_008360.2:g.40582_40602dup, NG_008360.2:g.40581_40602dup, NG_008360.2:g.40580_40602dup, NG_008360.2:g.40602_40603insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008360.2:g.40602_40603insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                                    18.

                                    rs1491000919 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      5:126832824 (GRCh38)
                                      5:126168516 (GRCh37)
                                      Canonical SPDI:
                                      NC_000005.10:126832823:T:C
                                      Gene:
                                      LMNB1 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_downstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000005/1 (GnomAD_exomes)
                                      C=0.000008/2 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1490905653 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        5:126828498 (GRCh38)
                                        5:126164190 (GRCh37)
                                        Canonical SPDI:
                                        NC_000005.10:126828497:T:C
                                        Gene:
                                        LMNB1 (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        C=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1490846866 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          5:126812405 (GRCh38)
                                          5:126148097 (GRCh37)
                                          Canonical SPDI:
                                          NC_000005.10:126812404:G:A
                                          Gene:
                                          LMNB1 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000007/1 (GnomAD)
                                          HGVS:

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