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Items: 1 to 20 of 16496

1.

rs1491588539 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->TAAAA [Show Flanks]
    Chromosome:
    1:200594369 (GRCh38)
    1:200563498 (GRCh37)
    Canonical SPDI:
    NC_000001.11:200594369:AAAA:AAAATAAAA
    Gene:
    KIF14 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

    2.

    rs1491569554 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CC>- [Show Flanks]
      Chromosome:
      1:200567169 (GRCh38)
      1:200536297 (GRCh37)
      Canonical SPDI:
      NC_000001.11:200567168:CC:
      Gene:
      KIF14 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by cluster
      MAF:
      -=0.0054/21 (ALSPAC)
      -=0.0067/25 (TWINSUK)
      HGVS:

      3.

      rs1491560641 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        TA>- [Show Flanks]
        Chromosome:
        1:200575824 (GRCh38)
        1:200544952 (GRCh37)
        Canonical SPDI:
        NC_000001.11:200575823:TA:
        Gene:
        KIF14 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        -=0./0 (ALFA)
        -=0.000004/1 (TOPMED)
        -=0.000007/1 (GnomAD)
        HGVS:

        4.

        rs1491557501 has merged into rs57476742 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          TTTTTTTTTTTTT>-,T,TT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
          Chromosome:
          1:200593936 (GRCh38)
          1:200563064 (GRCh37)
          Canonical SPDI:
          NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
          Gene:
          KIF14 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TTTTTTTTTT=0./0 (ALFA)
          HGVS:
          NC_000001.11:g.200593936_200593948del, NC_000001.11:g.200593937_200593948del, NC_000001.11:g.200593938_200593948del, NC_000001.11:g.200593945_200593948del, NC_000001.11:g.200593947_200593948del, NC_000001.11:g.200593948del, NC_000001.11:g.200593948dup, NC_000001.11:g.200593947_200593948dup, NC_000001.11:g.200593946_200593948dup, NC_000001.11:g.200593945_200593948dup, NC_000001.11:g.200593944_200593948dup, NC_000001.11:g.200593943_200593948dup, NC_000001.11:g.200593942_200593948dup, NC_000001.11:g.200593941_200593948dup, NC_000001.11:g.200593940_200593948dup, NC_000001.11:g.200593939_200593948dup, NC_000001.11:g.200593938_200593948dup, NC_000001.11:g.200593937_200593948dup, NC_000001.11:g.200593936_200593948dup, NC_000001.11:g.200593934_200593948dup, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563064_200563076del, NC_000001.10:g.200563065_200563076del, NC_000001.10:g.200563066_200563076del, NC_000001.10:g.200563073_200563076del, NC_000001.10:g.200563075_200563076del, NC_000001.10:g.200563076del, NC_000001.10:g.200563076dup, NC_000001.10:g.200563075_200563076dup, NC_000001.10:g.200563074_200563076dup, NC_000001.10:g.200563073_200563076dup, NC_000001.10:g.200563072_200563076dup, NC_000001.10:g.200563071_200563076dup, NC_000001.10:g.200563070_200563076dup, NC_000001.10:g.200563069_200563076dup, NC_000001.10:g.200563068_200563076dup, NC_000001.10:g.200563067_200563076dup, NC_000001.10:g.200563066_200563076dup, NC_000001.10:g.200563065_200563076dup, NC_000001.10:g.200563064_200563076dup, NC_000001.10:g.200563062_200563076dup, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042074.1:g.31795_31807del, NG_042074.1:g.31796_31807del, NG_042074.1:g.31797_31807del, NG_042074.1:g.31804_31807del, NG_042074.1:g.31806_31807del, NG_042074.1:g.31807del, NG_042074.1:g.31807dup, NG_042074.1:g.31806_31807dup, NG_042074.1:g.31805_31807dup, NG_042074.1:g.31804_31807dup, NG_042074.1:g.31803_31807dup, NG_042074.1:g.31802_31807dup, NG_042074.1:g.31801_31807dup, NG_042074.1:g.31800_31807dup, NG_042074.1:g.31799_31807dup, NG_042074.1:g.31798_31807dup, NG_042074.1:g.31797_31807dup, NG_042074.1:g.31796_31807dup, NG_042074.1:g.31795_31807dup, NG_042074.1:g.31793_31807dup, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

          5.

          rs1491534783 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->CTTT [Show Flanks]
            Chromosome:
            1:200623889 (GRCh38)
            1:200593018 (GRCh37)
            Canonical SPDI:
            NC_000001.11:200623889:TTT:TTTCTTT
            Validated:
            by frequency,by alfa
            MAF:
            TTTCTTT=0./0 (ALFA)
            TTTC=0.00003/2 (GnomAD)
            HGVS:

            6.

            rs1491507593 has merged into rs796133778 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              1:200623892 (GRCh38)
              1:200593020 (GRCh37)
              Canonical SPDI:
              NC_000001.11:200623888:TTTTTT:TTT,NC_000001.11:200623888:TTTTTT:TTTT,NC_000001.11:200623888:TTTTTT:TTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200623888:TTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTT=0./0 (ALFA)
              -=0.000008/2 (TOPMED)
              HGVS:
              NC_000001.11:g.200623892_200623894del, NC_000001.11:g.200623893_200623894del, NC_000001.11:g.200623894del, NC_000001.11:g.200623894dup, NC_000001.11:g.200623893_200623894dup, NC_000001.11:g.200623892_200623894dup, NC_000001.11:g.200623891_200623894dup, NC_000001.11:g.200623890_200623894dup, NC_000001.11:g.200623889_200623894dup, NC_000001.11:g.200623894_200623895insTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200623894_200623895insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593020_200593022del, NC_000001.10:g.200593021_200593022del, NC_000001.10:g.200593022del, NC_000001.10:g.200593022dup, NC_000001.10:g.200593021_200593022dup, NC_000001.10:g.200593020_200593022dup, NC_000001.10:g.200593019_200593022dup, NC_000001.10:g.200593018_200593022dup, NC_000001.10:g.200593017_200593022dup, NC_000001.10:g.200593022_200593023insTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200593022_200593023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042074.1:g.1844_1846del, NG_042074.1:g.1845_1846del, NG_042074.1:g.1846del, NG_042074.1:g.1846dup, NG_042074.1:g.1845_1846dup, NG_042074.1:g.1844_1846dup, NG_042074.1:g.1843_1846dup, NG_042074.1:g.1842_1846dup, NG_042074.1:g.1841_1846dup, NG_042074.1:g.1846_1847insAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.1846_1847insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

              7.

              rs1491380822 has merged into rs66935478 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTCCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                1:200581772 (GRCh38)
                1:200550900 (GRCh37)
                Canonical SPDI:
                NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                Gene:
                KIF14 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTTTTTTTTT=0./0 (ALFA)
                -=0.35/14 (GENOME_DK)
                HGVS:
                NC_000001.11:g.200581772_200581784del, NC_000001.11:g.200581773_200581784del, NC_000001.11:g.200581776_200581784del, NC_000001.11:g.200581777_200581784del, NC_000001.11:g.200581778_200581784del, NC_000001.11:g.200581779_200581784del, NC_000001.11:g.200581780_200581784del, NC_000001.11:g.200581781_200581784del, NC_000001.11:g.200581782_200581784del, NC_000001.11:g.200581783_200581784del, NC_000001.11:g.200581784del, NC_000001.11:g.200581784dup, NC_000001.11:g.200581783_200581784dup, NC_000001.11:g.200581782_200581784dup, NC_000001.11:g.200581781_200581784dup, NC_000001.11:g.200581762_200581784T[27]CCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.200581780_200581784dup, NC_000001.11:g.200581779_200581784dup, NC_000001.11:g.200581778_200581784dup, NC_000001.11:g.200581777_200581784dup, NC_000001.11:g.200581776_200581784dup, NC_000001.11:g.200581772_200581784dup, NC_000001.11:g.200581771_200581784dup, NC_000001.11:g.200581767_200581784dup, NC_000001.11:g.200581762_200581784dup, NC_000001.10:g.200550900_200550912del, NC_000001.10:g.200550901_200550912del, NC_000001.10:g.200550904_200550912del, NC_000001.10:g.200550905_200550912del, NC_000001.10:g.200550906_200550912del, NC_000001.10:g.200550907_200550912del, NC_000001.10:g.200550908_200550912del, NC_000001.10:g.200550909_200550912del, NC_000001.10:g.200550910_200550912del, NC_000001.10:g.200550911_200550912del, NC_000001.10:g.200550912del, NC_000001.10:g.200550912dup, NC_000001.10:g.200550911_200550912dup, NC_000001.10:g.200550910_200550912dup, NC_000001.10:g.200550909_200550912dup, NC_000001.10:g.200550890_200550912T[27]CCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.200550908_200550912dup, NC_000001.10:g.200550907_200550912dup, NC_000001.10:g.200550906_200550912dup, NC_000001.10:g.200550905_200550912dup, NC_000001.10:g.200550904_200550912dup, NC_000001.10:g.200550900_200550912dup, NC_000001.10:g.200550899_200550912dup, NC_000001.10:g.200550895_200550912dup, NC_000001.10:g.200550890_200550912dup, NG_042074.1:g.43961_43973del, NG_042074.1:g.43962_43973del, NG_042074.1:g.43965_43973del, NG_042074.1:g.43966_43973del, NG_042074.1:g.43967_43973del, NG_042074.1:g.43968_43973del, NG_042074.1:g.43969_43973del, NG_042074.1:g.43970_43973del, NG_042074.1:g.43971_43973del, NG_042074.1:g.43972_43973del, NG_042074.1:g.43973del, NG_042074.1:g.43973dup, NG_042074.1:g.43972_43973dup, NG_042074.1:g.43971_43973dup, NG_042074.1:g.43970_43973dup, NG_042074.1:g.43951_43973A[24]GACCAGGAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.43969_43973dup, NG_042074.1:g.43968_43973dup, NG_042074.1:g.43967_43973dup, NG_042074.1:g.43966_43973dup, NG_042074.1:g.43965_43973dup, NG_042074.1:g.43961_43973dup, NG_042074.1:g.43960_43973dup, NG_042074.1:g.43956_43973dup, NG_042074.1:g.43951_43973dup

                8.

                rs1491374765 has merged into rs35647787 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
                  Chromosome:
                  1:200610521 (GRCh38)
                  1:200579649 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                  Gene:
                  KIF14 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAAAAAAAAAAAA=0./0 (ALFA)
                  AAA=0.000004/1 (TOPMED)
                  A=0.398762/1997 (1000Genomes)
                  HGVS:
                  NC_000001.11:g.200610521_200610530del, NC_000001.11:g.200610523_200610530del, NC_000001.11:g.200610525_200610530del, NC_000001.11:g.200610526_200610530del, NC_000001.11:g.200610527_200610530del, NC_000001.11:g.200610528_200610530del, NC_000001.11:g.200610529_200610530del, NC_000001.11:g.200610530del, NC_000001.11:g.200610530dup, NC_000001.11:g.200610528_200610530dup, NC_000001.11:g.200610523_200610530dup, NC_000001.10:g.200579649_200579658del, NC_000001.10:g.200579651_200579658del, NC_000001.10:g.200579653_200579658del, NC_000001.10:g.200579654_200579658del, NC_000001.10:g.200579655_200579658del, NC_000001.10:g.200579656_200579658del, NC_000001.10:g.200579657_200579658del, NC_000001.10:g.200579658del, NC_000001.10:g.200579658dup, NC_000001.10:g.200579656_200579658dup, NC_000001.10:g.200579651_200579658dup, NG_042074.1:g.15216_15225del, NG_042074.1:g.15218_15225del, NG_042074.1:g.15220_15225del, NG_042074.1:g.15221_15225del, NG_042074.1:g.15222_15225del, NG_042074.1:g.15223_15225del, NG_042074.1:g.15224_15225del, NG_042074.1:g.15225del, NG_042074.1:g.15225dup, NG_042074.1:g.15223_15225dup, NG_042074.1:g.15218_15225dup

                  9.

                  rs1491346221 [Homo sapiens]
                    Variant type:
                    INS
                    Alleles:
                    ->TTTA [Show Flanks]
                    Chromosome:
                    1:200574960 (GRCh38)
                    1:200544089 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:200574960::TTTA
                    Gene:
                    KIF14 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    TTTA=0.0002/1 (ALFA)
                    HGVS:

                    10.

                    rs1491296790 has merged into rs371729211 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                      Chromosome:
                      1:200594380 (GRCh38)
                      1:200563508 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA
                      Gene:
                      KIF14 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAAAAAAAA=0./0 (ALFA)
                      HGVS:
                      NC_000001.11:g.200594380_200594393del, NC_000001.11:g.200594381_200594393del, NC_000001.11:g.200594382_200594393del, NC_000001.11:g.200594383_200594393del, NC_000001.11:g.200594384_200594393del, NC_000001.11:g.200594385_200594393del, NC_000001.11:g.200594386_200594393del, NC_000001.11:g.200594387_200594393del, NC_000001.11:g.200594388_200594393del, NC_000001.11:g.200594389_200594393del, NC_000001.11:g.200594390_200594393del, NC_000001.11:g.200594391_200594393del, NC_000001.11:g.200594392_200594393del, NC_000001.11:g.200594393del, NC_000001.11:g.200594393dup, NC_000001.11:g.200594392_200594393dup, NC_000001.11:g.200594391_200594393dup, NC_000001.11:g.200594390_200594393dup, NC_000001.11:g.200594389_200594393dup, NC_000001.11:g.200594388_200594393dup, NC_000001.11:g.200594387_200594393dup, NC_000001.11:g.200594386_200594393dup, NC_000001.11:g.200594385_200594393dup, NC_000001.11:g.200594384_200594393dup, NC_000001.11:g.200594383_200594393dup, NC_000001.11:g.200594382_200594393dup, NC_000001.11:g.200594380_200594393dup, NC_000001.11:g.200594379_200594393dup, NC_000001.11:g.200594378_200594393dup, NC_000001.11:g.200594377_200594393dup, NC_000001.11:g.200594369_200594393A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.200563508_200563521del, NC_000001.10:g.200563509_200563521del, NC_000001.10:g.200563510_200563521del, NC_000001.10:g.200563511_200563521del, NC_000001.10:g.200563512_200563521del, NC_000001.10:g.200563513_200563521del, NC_000001.10:g.200563514_200563521del, NC_000001.10:g.200563515_200563521del, NC_000001.10:g.200563516_200563521del, NC_000001.10:g.200563517_200563521del, NC_000001.10:g.200563518_200563521del, NC_000001.10:g.200563519_200563521del, NC_000001.10:g.200563520_200563521del, NC_000001.10:g.200563521del, NC_000001.10:g.200563521dup, NC_000001.10:g.200563520_200563521dup, NC_000001.10:g.200563519_200563521dup, NC_000001.10:g.200563518_200563521dup, NC_000001.10:g.200563517_200563521dup, NC_000001.10:g.200563516_200563521dup, NC_000001.10:g.200563515_200563521dup, NC_000001.10:g.200563514_200563521dup, NC_000001.10:g.200563513_200563521dup, NC_000001.10:g.200563512_200563521dup, NC_000001.10:g.200563511_200563521dup, NC_000001.10:g.200563510_200563521dup, NC_000001.10:g.200563508_200563521dup, NC_000001.10:g.200563507_200563521dup, NC_000001.10:g.200563506_200563521dup, NC_000001.10:g.200563505_200563521dup, NC_000001.10:g.200563497_200563521A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.31353_31366del, NG_042074.1:g.31354_31366del, NG_042074.1:g.31355_31366del, NG_042074.1:g.31356_31366del, NG_042074.1:g.31357_31366del, NG_042074.1:g.31358_31366del, NG_042074.1:g.31359_31366del, NG_042074.1:g.31360_31366del, NG_042074.1:g.31361_31366del, NG_042074.1:g.31362_31366del, NG_042074.1:g.31363_31366del, NG_042074.1:g.31364_31366del, NG_042074.1:g.31365_31366del, NG_042074.1:g.31366del, NG_042074.1:g.31366dup, NG_042074.1:g.31365_31366dup, NG_042074.1:g.31364_31366dup, NG_042074.1:g.31363_31366dup, NG_042074.1:g.31362_31366dup, NG_042074.1:g.31361_31366dup, NG_042074.1:g.31360_31366dup, NG_042074.1:g.31359_31366dup, NG_042074.1:g.31358_31366dup, NG_042074.1:g.31357_31366dup, NG_042074.1:g.31356_31366dup, NG_042074.1:g.31355_31366dup, NG_042074.1:g.31353_31366dup, NG_042074.1:g.31352_31366dup, NG_042074.1:g.31351_31366dup, NG_042074.1:g.31350_31366dup, NG_042074.1:g.31342_31366T[26]ATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

                      11.

                      rs1491282916 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        CA>- [Show Flanks]
                        Chromosome:
                        1:200610509 (GRCh38)
                        1:200579637 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:200610508:CA:
                        Gene:
                        KIF14 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        -=0.00084/10 (ALFA)
                        HGVS:

                        12.

                        rs1491279226 has merged into rs371729211 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                          Chromosome:
                          1:200594380 (GRCh38)
                          1:200563508 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA
                          Gene:
                          KIF14 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          AAAAAAAAAAA=0./0 (ALFA)
                          HGVS:
                          NC_000001.11:g.200594380_200594393del, NC_000001.11:g.200594381_200594393del, NC_000001.11:g.200594382_200594393del, NC_000001.11:g.200594383_200594393del, NC_000001.11:g.200594384_200594393del, NC_000001.11:g.200594385_200594393del, NC_000001.11:g.200594386_200594393del, NC_000001.11:g.200594387_200594393del, NC_000001.11:g.200594388_200594393del, NC_000001.11:g.200594389_200594393del, NC_000001.11:g.200594390_200594393del, NC_000001.11:g.200594391_200594393del, NC_000001.11:g.200594392_200594393del, NC_000001.11:g.200594393del, NC_000001.11:g.200594393dup, NC_000001.11:g.200594392_200594393dup, NC_000001.11:g.200594391_200594393dup, NC_000001.11:g.200594390_200594393dup, NC_000001.11:g.200594389_200594393dup, NC_000001.11:g.200594388_200594393dup, NC_000001.11:g.200594387_200594393dup, NC_000001.11:g.200594386_200594393dup, NC_000001.11:g.200594385_200594393dup, NC_000001.11:g.200594384_200594393dup, NC_000001.11:g.200594383_200594393dup, NC_000001.11:g.200594382_200594393dup, NC_000001.11:g.200594380_200594393dup, NC_000001.11:g.200594379_200594393dup, NC_000001.11:g.200594378_200594393dup, NC_000001.11:g.200594377_200594393dup, NC_000001.11:g.200594369_200594393A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.200563508_200563521del, NC_000001.10:g.200563509_200563521del, NC_000001.10:g.200563510_200563521del, NC_000001.10:g.200563511_200563521del, NC_000001.10:g.200563512_200563521del, NC_000001.10:g.200563513_200563521del, NC_000001.10:g.200563514_200563521del, NC_000001.10:g.200563515_200563521del, NC_000001.10:g.200563516_200563521del, NC_000001.10:g.200563517_200563521del, NC_000001.10:g.200563518_200563521del, NC_000001.10:g.200563519_200563521del, NC_000001.10:g.200563520_200563521del, NC_000001.10:g.200563521del, NC_000001.10:g.200563521dup, NC_000001.10:g.200563520_200563521dup, NC_000001.10:g.200563519_200563521dup, NC_000001.10:g.200563518_200563521dup, NC_000001.10:g.200563517_200563521dup, NC_000001.10:g.200563516_200563521dup, NC_000001.10:g.200563515_200563521dup, NC_000001.10:g.200563514_200563521dup, NC_000001.10:g.200563513_200563521dup, NC_000001.10:g.200563512_200563521dup, NC_000001.10:g.200563511_200563521dup, NC_000001.10:g.200563510_200563521dup, NC_000001.10:g.200563508_200563521dup, NC_000001.10:g.200563507_200563521dup, NC_000001.10:g.200563506_200563521dup, NC_000001.10:g.200563505_200563521dup, NC_000001.10:g.200563497_200563521A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.31353_31366del, NG_042074.1:g.31354_31366del, NG_042074.1:g.31355_31366del, NG_042074.1:g.31356_31366del, NG_042074.1:g.31357_31366del, NG_042074.1:g.31358_31366del, NG_042074.1:g.31359_31366del, NG_042074.1:g.31360_31366del, NG_042074.1:g.31361_31366del, NG_042074.1:g.31362_31366del, NG_042074.1:g.31363_31366del, NG_042074.1:g.31364_31366del, NG_042074.1:g.31365_31366del, NG_042074.1:g.31366del, NG_042074.1:g.31366dup, NG_042074.1:g.31365_31366dup, NG_042074.1:g.31364_31366dup, NG_042074.1:g.31363_31366dup, NG_042074.1:g.31362_31366dup, NG_042074.1:g.31361_31366dup, NG_042074.1:g.31360_31366dup, NG_042074.1:g.31359_31366dup, NG_042074.1:g.31358_31366dup, NG_042074.1:g.31357_31366dup, NG_042074.1:g.31356_31366dup, NG_042074.1:g.31355_31366dup, NG_042074.1:g.31353_31366dup, NG_042074.1:g.31352_31366dup, NG_042074.1:g.31351_31366dup, NG_042074.1:g.31350_31366dup, NG_042074.1:g.31342_31366T[26]ATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

                          13.

                          rs1491262516 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            ->A [Show Flanks]
                            Chromosome:
                            1:200575824 (GRCh38)
                            1:200544953 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:200575824:AAAAAA:AAAAAAA
                            Gene:
                            KIF14 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            AAAAAAA=0.000071/1 (ALFA)
                            A=0.000011/3 (TOPMED)
                            A=0.000014/2 (GnomAD)
                            HGVS:

                            14.

                            rs1491256377 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              ->AAGACTCTG [Show Flanks]
                              Chromosome:
                              1:200564625 (GRCh38)
                              1:200533754 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:200564625:AAGACTCTG:AAGACTCTGAAGACTCTG
                              Gene:
                              KIF14 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              AAGACTCTGAAGACTCTG=0./0 (ALFA)
                              AAGACTCTG=0.000014/2 (GnomAD)
                              HGVS:

                              15.

                              rs1491164469 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                CA>- [Show Flanks]
                                Chromosome:
                                1:200594368 (GRCh38)
                                1:200563496 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:200594367:CA:
                                Gene:
                                KIF14 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                -=0.00194/23 (ALFA)
                                -=0.00589/81 (GnomAD)
                                HGVS:

                                16.

                                rs1491108451 has merged into rs993346438 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                  Chromosome:
                                  1:200596901 (GRCh38)
                                  1:200566029 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                  Gene:
                                  KIF14 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TTTTTTTTTTTT=0./0 (ALFA)
                                  HGVS:
                                  NC_000001.11:g.200596901_200596913del, NC_000001.11:g.200596902_200596913del, NC_000001.11:g.200596903_200596913del, NC_000001.11:g.200596904_200596913del, NC_000001.11:g.200596905_200596913del, NC_000001.11:g.200596906_200596913del, NC_000001.11:g.200596907_200596913del, NC_000001.11:g.200596908_200596913del, NC_000001.11:g.200596909_200596913del, NC_000001.11:g.200596910_200596913del, NC_000001.11:g.200596911_200596913del, NC_000001.11:g.200596912_200596913del, NC_000001.11:g.200596913del, NC_000001.11:g.200596913dup, NC_000001.11:g.200596912_200596913dup, NC_000001.11:g.200596911_200596913dup, NC_000001.11:g.200596910_200596913dup, NC_000001.11:g.200596909_200596913dup, NC_000001.11:g.200596908_200596913dup, NC_000001.11:g.200596907_200596913dup, NC_000001.11:g.200596905_200596913dup, NC_000001.11:g.200596900_200596913dup, NC_000001.11:g.200596913_200596914insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200596913_200596914insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200566029_200566041del, NC_000001.10:g.200566030_200566041del, NC_000001.10:g.200566031_200566041del, NC_000001.10:g.200566032_200566041del, NC_000001.10:g.200566033_200566041del, NC_000001.10:g.200566034_200566041del, NC_000001.10:g.200566035_200566041del, NC_000001.10:g.200566036_200566041del, NC_000001.10:g.200566037_200566041del, NC_000001.10:g.200566038_200566041del, NC_000001.10:g.200566039_200566041del, NC_000001.10:g.200566040_200566041del, NC_000001.10:g.200566041del, NC_000001.10:g.200566041dup, NC_000001.10:g.200566040_200566041dup, NC_000001.10:g.200566039_200566041dup, NC_000001.10:g.200566038_200566041dup, NC_000001.10:g.200566037_200566041dup, NC_000001.10:g.200566036_200566041dup, NC_000001.10:g.200566035_200566041dup, NC_000001.10:g.200566033_200566041dup, NC_000001.10:g.200566028_200566041dup, NC_000001.10:g.200566041_200566042insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200566041_200566042insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042074.1:g.28834_28846del, NG_042074.1:g.28835_28846del, NG_042074.1:g.28836_28846del, NG_042074.1:g.28837_28846del, NG_042074.1:g.28838_28846del, NG_042074.1:g.28839_28846del, NG_042074.1:g.28840_28846del, NG_042074.1:g.28841_28846del, NG_042074.1:g.28842_28846del, NG_042074.1:g.28843_28846del, NG_042074.1:g.28844_28846del, NG_042074.1:g.28845_28846del, NG_042074.1:g.28846del, NG_042074.1:g.28846dup, NG_042074.1:g.28845_28846dup, NG_042074.1:g.28844_28846dup, NG_042074.1:g.28843_28846dup, NG_042074.1:g.28842_28846dup, NG_042074.1:g.28841_28846dup, NG_042074.1:g.28840_28846dup, NG_042074.1:g.28838_28846dup, NG_042074.1:g.28833_28846dup, NG_042074.1:g.28846_28847insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.28846_28847insAAAAAAAAAAAAAAAAAAAAAAAAAAA

                                  17.

                                  rs1491090568 [Homo sapiens]
                                    Variant type:
                                    DEL
                                    Alleles:
                                    TG>- [Show Flanks]
                                    Chromosome:
                                    1:200574960 (GRCh38)
                                    1:200544088 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:200574959:TG:
                                    Gene:
                                    KIF14 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    -=0.00042/5 (ALFA)
                                    HGVS:

                                    18.

                                    rs1491083938 has merged into rs10643609 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
                                      Chromosome:
                                      1:200561239 (GRCh38)
                                      1:200530367 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
                                      Gene:
                                      KIF14 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      AAAAAAAAAA=0./0 (ALFA)
                                      -=0.2722/1363 (1000Genomes)
                                      -=0.3/12 (GENOME_DK)
                                      HGVS:
                                      NC_000001.11:g.200561239_200561244del, NC_000001.11:g.200561240_200561244del, NC_000001.11:g.200561241_200561244del, NC_000001.11:g.200561242_200561244del, NC_000001.11:g.200561243_200561244del, NC_000001.11:g.200561244del, NC_000001.11:g.200561244dup, NC_000001.11:g.200561243_200561244dup, NC_000001.11:g.200561242_200561244dup, NC_000001.11:g.200561241_200561244dup, NC_000001.11:g.200561240_200561244dup, NC_000001.11:g.200561239_200561244dup, NC_000001.11:g.200561238_200561244dup, NC_000001.11:g.200561237_200561244dup, NC_000001.11:g.200561236_200561244dup, NC_000001.11:g.200561235_200561244dup, NC_000001.10:g.200530367_200530372del, NC_000001.10:g.200530368_200530372del, NC_000001.10:g.200530369_200530372del, NC_000001.10:g.200530370_200530372del, NC_000001.10:g.200530371_200530372del, NC_000001.10:g.200530372del, NC_000001.10:g.200530372dup, NC_000001.10:g.200530371_200530372dup, NC_000001.10:g.200530370_200530372dup, NC_000001.10:g.200530369_200530372dup, NC_000001.10:g.200530368_200530372dup, NC_000001.10:g.200530367_200530372dup, NC_000001.10:g.200530366_200530372dup, NC_000001.10:g.200530365_200530372dup, NC_000001.10:g.200530364_200530372dup, NC_000001.10:g.200530363_200530372dup, NG_042074.1:g.64500_64505del, NG_042074.1:g.64501_64505del, NG_042074.1:g.64502_64505del, NG_042074.1:g.64503_64505del, NG_042074.1:g.64504_64505del, NG_042074.1:g.64505del, NG_042074.1:g.64505dup, NG_042074.1:g.64504_64505dup, NG_042074.1:g.64503_64505dup, NG_042074.1:g.64502_64505dup, NG_042074.1:g.64501_64505dup, NG_042074.1:g.64500_64505dup, NG_042074.1:g.64499_64505dup, NG_042074.1:g.64498_64505dup, NG_042074.1:g.64497_64505dup, NG_042074.1:g.64496_64505dup

                                      19.

                                      rs1491070639 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        CT>- [Show Flanks]
                                        Chromosome:
                                        1:200623895 (GRCh38)
                                        1:200593023 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:200623893:TCT:T
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        T=0.00143/17 (ALFA)
                                        -=0.00195/181 (GnomAD)
                                        -=0.00555/10 (Korea1K)
                                        HGVS:

                                        20.

                                        rs1491054356 has merged into rs79821962 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
                                          Chromosome:
                                          1:200612010 (GRCh38)
                                          1:200581138 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
                                          Gene:
                                          KIF14 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TTTTTTTTTT=0./0 (ALFA)
                                          T=0.1692/310 (Korea1K)
                                          T=0.3145/1575 (1000Genomes)
                                          T=0.325/13 (GENOME_DK)
                                          T=0.3278/196 (NorthernSweden)
                                          T=0.3379/1253 (TWINSUK)
                                          T=0.3415/1316 (ALSPAC)
                                          HGVS:
                                          NC_000001.11:g.200612010_200612011del, NC_000001.11:g.200612011del, NC_000001.11:g.200612011dup, NC_000001.11:g.200612010_200612011dup, NC_000001.11:g.200612009_200612011dup, NC_000001.11:g.200612008_200612011dup, NC_000001.11:g.200612007_200612011dup, NC_000001.11:g.200612006_200612011dup, NC_000001.11:g.200612005_200612011dup, NC_000001.11:g.200612004_200612011dup, NC_000001.11:g.200612001_200612011dup, NC_000001.11:g.200612011_200612012insTTTTTTTTTTTTT, NC_000001.11:g.200612011_200612012insTTTTTTTTTTTTTT, NC_000001.10:g.200581138_200581139del, NC_000001.10:g.200581139del, NC_000001.10:g.200581139dup, NC_000001.10:g.200581138_200581139dup, NC_000001.10:g.200581137_200581139dup, NC_000001.10:g.200581136_200581139dup, NC_000001.10:g.200581135_200581139dup, NC_000001.10:g.200581134_200581139dup, NC_000001.10:g.200581133_200581139dup, NC_000001.10:g.200581132_200581139dup, NC_000001.10:g.200581129_200581139dup, NC_000001.10:g.200581139_200581140insTTTTTTTTTTTTT, NC_000001.10:g.200581139_200581140insTTTTTTTTTTTTTT, NG_042074.1:g.13733_13734del, NG_042074.1:g.13734del, NG_042074.1:g.13734dup, NG_042074.1:g.13733_13734dup, NG_042074.1:g.13732_13734dup, NG_042074.1:g.13731_13734dup, NG_042074.1:g.13730_13734dup, NG_042074.1:g.13729_13734dup, NG_042074.1:g.13728_13734dup, NG_042074.1:g.13727_13734dup, NG_042074.1:g.13724_13734dup, NG_042074.1:g.13734_13735insAAAAAAAAAAAAA, NG_042074.1:g.13734_13735insAAAAAAAAAAAAAA

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