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Items: 1 to 20 of 9327

1.

rs1491582886 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->CTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    10:38202881 (GRCh38)
    10:38491810 (GRCh37)
    Canonical SPDI:
    NC_000010.11:38202881:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTT
    Gene:
    CCNYL4 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

    2.

    rs1491532366 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->C [Show Flanks]
      Chromosome:
      10:38197891 (GRCh38)
      10:38486820 (GRCh37)
      Canonical SPDI:
      NC_000010.11:38197891:C:CC
      Gene:
      CCNYL4 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      CC=0./0 (ALFA)
      C=0.000004/1 (TOPMED)
      HGVS:

      3.

      rs1491505851 has merged into rs67882330 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        10:38214537 (GRCh38)
        10:38503465 (GRCh37)
        Canonical SPDI:
        NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38214526:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        CCNYL4 (Varview)
        Functional Consequence:
        downstream_transcript_variant,500B_downstream_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTTTTTTTTTT=0./0 (ALFA)
        -=0.3456/1731 (1000Genomes)
        HGVS:
        NC_000010.11:g.38214537_38214546del, NC_000010.11:g.38214538_38214546del, NC_000010.11:g.38214540_38214546del, NC_000010.11:g.38214541_38214546del, NC_000010.11:g.38214542_38214546del, NC_000010.11:g.38214543_38214546del, NC_000010.11:g.38214544_38214546del, NC_000010.11:g.38214545_38214546del, NC_000010.11:g.38214546del, NC_000010.11:g.38214546dup, NC_000010.11:g.38214545_38214546dup, NC_000010.11:g.38214544_38214546dup, NC_000010.11:g.38214543_38214546dup, NC_000010.11:g.38214542_38214546dup, NC_000010.11:g.38214541_38214546dup, NC_000010.11:g.38214540_38214546dup, NC_000010.11:g.38214539_38214546dup, NC_000010.11:g.38214537_38214546dup, NC_000010.11:g.38214536_38214546dup, NC_000010.11:g.38214534_38214546dup, NC_000010.11:g.38214533_38214546dup, NC_000010.11:g.38214546_38214547insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.38214546_38214547insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.38214546_38214547insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.38503465_38503474del, NC_000010.10:g.38503466_38503474del, NC_000010.10:g.38503468_38503474del, NC_000010.10:g.38503469_38503474del, NC_000010.10:g.38503470_38503474del, NC_000010.10:g.38503471_38503474del, NC_000010.10:g.38503472_38503474del, NC_000010.10:g.38503473_38503474del, NC_000010.10:g.38503474del, NC_000010.10:g.38503474dup, NC_000010.10:g.38503473_38503474dup, NC_000010.10:g.38503472_38503474dup, NC_000010.10:g.38503471_38503474dup, NC_000010.10:g.38503470_38503474dup, NC_000010.10:g.38503469_38503474dup, NC_000010.10:g.38503468_38503474dup, NC_000010.10:g.38503467_38503474dup, NC_000010.10:g.38503465_38503474dup, NC_000010.10:g.38503464_38503474dup, NC_000010.10:g.38503462_38503474dup, NC_000010.10:g.38503461_38503474dup, NC_000010.10:g.38503474_38503475insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.38503474_38503475insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.38503474_38503475insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

        4.

        rs1491460329 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          CT>- [Show Flanks]
          Chromosome:
          10:38197892 (GRCh38)
          10:38486820 (GRCh37)
          Canonical SPDI:
          NC_000010.11:38197890:TCT:T
          Gene:
          CCNYL4 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.00051/6 (ALFA)
          -=0.00004/1 (TOMMO)
          HGVS:

          5.

          rs1491369758 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            TG>- [Show Flanks]
            Chromosome:
            10:38180769 (GRCh38)
            10:38469697 (GRCh37)
            Canonical SPDI:
            NC_000010.11:38180768:TG:
            Gene:
            CCNYL4 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            -=0.00025/3 (ALFA)
            HGVS:

            6.

            rs1491305038 has merged into rs113460282 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              CA>-,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA [Show Flanks]
              Chromosome:
              10:38208302 (GRCh38)
              10:38497230 (GRCh37)
              Canonical SPDI:
              NC_000010.11:38208292:ACACACACACA:ACACACACA,NC_000010.11:38208292:ACACACACACA:ACACACACACACA,NC_000010.11:38208292:ACACACACACA:ACACACACACACACA,NC_000010.11:38208292:ACACACACACA:ACACACACACACACACA,NC_000010.11:38208292:ACACACACACA:ACACACACACACACACACA,NC_000010.11:38208292:ACACACACACA:ACACACACACACACACACACA
              Gene:
              CCNYL4 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              ACACACACACACACACA=0./0 (ALFA)
              AC=0.3983/239 (NorthernSweden)
              AC=0.45/18 (GENOME_DK)
              HGVS:

              7.

              rs1491296623 has merged into rs5784568 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                10:38202891 (GRCh38)
                10:38491819 (GRCh37)
                Canonical SPDI:
                NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38202880:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                Gene:
                CCNYL4 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTTTTTTTT=0./0 (ALFA)
                -=0.000008/2 (TOPMED)
                HGVS:
                NC_000010.11:g.38202891_38202901del, NC_000010.11:g.38202892_38202901del, NC_000010.11:g.38202893_38202901del, NC_000010.11:g.38202894_38202901del, NC_000010.11:g.38202895_38202901del, NC_000010.11:g.38202897_38202901del, NC_000010.11:g.38202898_38202901del, NC_000010.11:g.38202899_38202901del, NC_000010.11:g.38202900_38202901del, NC_000010.11:g.38202901del, NC_000010.11:g.38202901dup, NC_000010.11:g.38202900_38202901dup, NC_000010.11:g.38202899_38202901dup, NC_000010.11:g.38202898_38202901dup, NC_000010.11:g.38202896_38202901dup, NC_000010.11:g.38202894_38202901dup, NC_000010.11:g.38202901_38202902insTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.38202901_38202902insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.38491819_38491829del, NC_000010.10:g.38491820_38491829del, NC_000010.10:g.38491821_38491829del, NC_000010.10:g.38491822_38491829del, NC_000010.10:g.38491823_38491829del, NC_000010.10:g.38491825_38491829del, NC_000010.10:g.38491826_38491829del, NC_000010.10:g.38491827_38491829del, NC_000010.10:g.38491828_38491829del, NC_000010.10:g.38491829del, NC_000010.10:g.38491829dup, NC_000010.10:g.38491828_38491829dup, NC_000010.10:g.38491827_38491829dup, NC_000010.10:g.38491826_38491829dup, NC_000010.10:g.38491824_38491829dup, NC_000010.10:g.38491822_38491829dup, NC_000010.10:g.38491829_38491830insTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.38491829_38491830insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                8.

                rs1491287592 has merged into rs3041933 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  10:38180760 (GRCh38)
                  10:38469688 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:38180750:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  CCNYL4 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTT=0./0 (ALFA)
                  -=0.000004/1 (TOPMED)
                  -=0.26238/1314 (1000Genomes)
                  HGVS:
                  NC_000010.11:g.38180760_38180769del, NC_000010.11:g.38180761_38180769del, NC_000010.11:g.38180762_38180769del, NC_000010.11:g.38180763_38180769del, NC_000010.11:g.38180764_38180769del, NC_000010.11:g.38180765_38180769del, NC_000010.11:g.38180766_38180769del, NC_000010.11:g.38180767_38180769del, NC_000010.11:g.38180768_38180769del, NC_000010.11:g.38180769del, NC_000010.11:g.38180769dup, NC_000010.11:g.38180768_38180769dup, NC_000010.11:g.38180767_38180769dup, NC_000010.11:g.38180766_38180769dup, NC_000010.11:g.38180765_38180769dup, NC_000010.11:g.38180764_38180769dup, NC_000010.11:g.38180763_38180769dup, NC_000010.11:g.38180762_38180769dup, NC_000010.11:g.38180760_38180769dup, NC_000010.11:g.38180757_38180769dup, NC_000010.11:g.38180756_38180769dup, NC_000010.10:g.38469688_38469697del, NC_000010.10:g.38469689_38469697del, NC_000010.10:g.38469690_38469697del, NC_000010.10:g.38469691_38469697del, NC_000010.10:g.38469692_38469697del, NC_000010.10:g.38469693_38469697del, NC_000010.10:g.38469694_38469697del, NC_000010.10:g.38469695_38469697del, NC_000010.10:g.38469696_38469697del, NC_000010.10:g.38469697del, NC_000010.10:g.38469697dup, NC_000010.10:g.38469696_38469697dup, NC_000010.10:g.38469695_38469697dup, NC_000010.10:g.38469694_38469697dup, NC_000010.10:g.38469693_38469697dup, NC_000010.10:g.38469692_38469697dup, NC_000010.10:g.38469691_38469697dup, NC_000010.10:g.38469690_38469697dup, NC_000010.10:g.38469688_38469697dup, NC_000010.10:g.38469685_38469697dup, NC_000010.10:g.38469684_38469697dup

                  9.

                  rs1491283922 [Homo sapiens]
                    Variant type:
                    DEL
                    Alleles:
                    CT>- [Show Flanks]
                    Chromosome:
                    10:38177616 (GRCh38)
                    10:38466544 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:38177615:CT:
                    Gene:
                    CCNYL4 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    -=0.00042/5 (ALFA)
                    HGVS:

                    10.

                    rs1491161082 [Homo sapiens]
                      Variant type:
                      SNV:
                      Alleles:
                      CA>-
                      Chromosome:
                      no mapping
                      Canonical SPDI:

                      11.

                      rs1491137564 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->A,AA,AAA [Show Flanks]
                        Chromosome:
                        10:38185180 (GRCh38)
                        10:38474109 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:38185180:AA:AAA,NC_000010.11:38185180:AA:AAAA,NC_000010.11:38185180:AA:AAAAA
                        Gene:
                        CCNYL4 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        AAAA=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1491134183 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          AT>- [Show Flanks]
                          Chromosome:
                          10:38180750 (GRCh38)
                          10:38469678 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:38180749:AT:
                          Gene:
                          CCNYL4 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          -=0.00007/1 (ALFA)
                          -=0.00013/13 (GnomAD)
                          HGVS:

                          13.

                          rs1491096959 [Homo sapiens]
                            Variant type:
                            SNV:
                            Alleles:
                            TA>-
                            Chromosome:
                            no mapping
                            Canonical SPDI:

                            14.

                            rs1491035338 [Homo sapiens]
                              Variant type:
                              INS
                              Alleles:
                              ->T [Show Flanks]
                              Chromosome:
                              10:38179161 (GRCh38)
                              10:38468090 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:38179161::T
                              Gene:
                              CCNYL4 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              T=0.0029/13 (ALFA)
                              HGVS:

                              15.

                              rs1490840345 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>G [Show Flanks]
                                Chromosome:
                                10:38186339 (GRCh38)
                                10:38475267 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:38186338:T:G
                                Gene:
                                CCNYL4 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000011/3 (TOPMED)
                                HGVS:

                                16.

                                rs1490727819 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>A [Show Flanks]
                                  Chromosome:
                                  10:38187333 (GRCh38)
                                  10:38476261 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:38187332:T:A
                                  Gene:
                                  CCNYL4 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000008/2 (TOPMED)
                                  A=0.000014/2 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1490585344 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->T [Show Flanks]
                                    Chromosome:
                                    10:38202720 (GRCh38)
                                    10:38491649 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:38202720:TTTT:TTTTT
                                    Gene:
                                    CCNYL4 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    TTTTT=0./0 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490564120 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      10:38187804 (GRCh38)
                                      10:38476732 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:38187803:C:G
                                      Gene:
                                      CCNYL4 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0.000071/1 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490539271 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>T [Show Flanks]
                                        Chromosome:
                                        10:38202912 (GRCh38)
                                        10:38491840 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:38202911:G:T
                                        Gene:
                                        CCNYL4 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0.00705/115 (ALFA)
                                        T=0.00109/2 (Korea1K)
                                        T=0.013/38 (KOREAN)
                                        HGVS:

                                        20.

                                        rs1490522854 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>A [Show Flanks]
                                          Chromosome:
                                          10:38200721 (GRCh38)
                                          10:38489649 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:38200720:C:A
                                          Gene:
                                          CCNYL4 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000008/2 (TOPMED)
                                          A=0.000021/3 (GnomAD)
                                          HGVS:

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