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1.

rs1491588934 has merged into rs10649653 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAAAAAAAAAAA>-,A,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
    Chromosome:
    17:36134815 (GRCh38)
    17:34462197 (GRCh37)
    Canonical SPDI:
    NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36134804:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
    Gene:
    LOC101927369 (Varview), LOC107985055 (Varview)
    Functional Consequence:
    2KB_upstream_variant,downstream_transcript_variant,upstream_transcript_variant,intron_variant,genic_downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAAAA=0./0 (ALFA)
    HGVS:
    NC_000017.11:g.36134815_36134826del, NC_000017.11:g.36134816_36134826del, NC_000017.11:g.36134818_36134826del, NC_000017.11:g.36134820_36134826del, NC_000017.11:g.36134821_36134826del, NC_000017.11:g.36134822_36134826del, NC_000017.11:g.36134823_36134826del, NC_000017.11:g.36134824_36134826del, NC_000017.11:g.36134825_36134826del, NC_000017.11:g.36134826del, NC_000017.11:g.36134826dup, NC_000017.11:g.36134825_36134826dup, NC_000017.11:g.36134824_36134826dup, NC_000017.11:g.36134823_36134826dup, NC_000017.11:g.36134822_36134826dup, NC_000017.11:g.36134821_36134826dup, NC_000017.11:g.36134820_36134826dup, NC_000017.11:g.36134819_36134826dup, NC_000017.11:g.36134818_36134826dup, NC_000017.11:g.36134817_36134826dup, NC_000017.11:g.36134816_36134826dup, NC_000017.11:g.36134815_36134826dup, NC_000017.11:g.36134814_36134826dup, NC_000017.11:g.36134813_36134826dup, NC_000017.11:g.36134812_36134826dup, NC_000017.11:g.36134811_36134826dup, NC_000017.11:g.36134810_36134826dup, NC_000017.11:g.36134809_36134826dup, NC_000017.11:g.36134826_36134827insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.11:g.36134826_36134827insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.11:g.36134826_36134827insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.11:g.36134826_36134827insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.369733_369734dup, NT_187614.1:g.369725_369734del, NT_187614.1:g.369726_369734del, NT_187614.1:g.369728_369734del, NT_187614.1:g.369730_369734del, NT_187614.1:g.369731_369734del, NT_187614.1:g.369732_369734del, NT_187614.1:g.369733_369734del, NT_187614.1:g.369734del, NT_187614.1:g.369734dup, NT_187614.1:g.369732_369734dup, NT_187614.1:g.369731_369734dup, NT_187614.1:g.369730_369734dup, NT_187614.1:g.369729_369734dup, NT_187614.1:g.369728_369734dup, NT_187614.1:g.369727_369734dup, NT_187614.1:g.369726_369734dup, NT_187614.1:g.369725_369734dup, NT_187614.1:g.369724_369734dup, NT_187614.1:g.369723_369734dup, NT_187614.1:g.369722_369734dup, NT_187614.1:g.369721_369734dup, NT_187614.1:g.369720_369734dup, NT_187614.1:g.369719_369734dup, NT_187614.1:g.369718_369734dup, NT_187614.1:g.369717_369734dup, NT_187614.1:g.369716_369734dup, NT_187614.1:g.369715_369734dup, NT_187614.1:g.369734_369735insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.369734_369735insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.369734_369735insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.369734_369735insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187661.1:g.88912_88923del, NT_187661.1:g.88913_88923del, NT_187661.1:g.88915_88923del, NT_187661.1:g.88917_88923del, NT_187661.1:g.88918_88923del, NT_187661.1:g.88919_88923del, NT_187661.1:g.88920_88923del, NT_187661.1:g.88921_88923del, NT_187661.1:g.88922_88923del, NT_187661.1:g.88923del, NT_187661.1:g.88923dup, NT_187661.1:g.88922_88923dup, NT_187661.1:g.88921_88923dup, NT_187661.1:g.88920_88923dup, NT_187661.1:g.88919_88923dup, NT_187661.1:g.88918_88923dup, NT_187661.1:g.88917_88923dup, NT_187661.1:g.88916_88923dup, NT_187661.1:g.88915_88923dup, NT_187661.1:g.88914_88923dup, NT_187661.1:g.88913_88923dup, NT_187661.1:g.88912_88923dup, NT_187661.1:g.88911_88923dup, NT_187661.1:g.88910_88923dup, NT_187661.1:g.88909_88923dup, NT_187661.1:g.88908_88923dup, NT_187661.1:g.88907_88923dup, NT_187661.1:g.88906_88923dup, NT_187661.1:g.88923_88924insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187661.1:g.88923_88924insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187661.1:g.88923_88924insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187661.1:g.88923_88924insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34462205_34462206dup, NC_000017.10:g.34462197_34462206del, NC_000017.10:g.34462198_34462206del, NC_000017.10:g.34462200_34462206del, NC_000017.10:g.34462202_34462206del, NC_000017.10:g.34462203_34462206del, NC_000017.10:g.34462204_34462206del, NC_000017.10:g.34462205_34462206del, NC_000017.10:g.34462206del, NC_000017.10:g.34462206dup, NC_000017.10:g.34462204_34462206dup, NC_000017.10:g.34462203_34462206dup, NC_000017.10:g.34462202_34462206dup, NC_000017.10:g.34462201_34462206dup, NC_000017.10:g.34462200_34462206dup, NC_000017.10:g.34462199_34462206dup, NC_000017.10:g.34462198_34462206dup, NC_000017.10:g.34462197_34462206dup, NC_000017.10:g.34462196_34462206dup, NC_000017.10:g.34462195_34462206dup, NC_000017.10:g.34462194_34462206dup, NC_000017.10:g.34462193_34462206dup, NC_000017.10:g.34462192_34462206dup, NC_000017.10:g.34462191_34462206dup, NC_000017.10:g.34462190_34462206dup, NC_000017.10:g.34462189_34462206dup, NC_000017.10:g.34462188_34462206dup, NC_000017.10:g.34462187_34462206dup, NC_000017.10:g.34462206_34462207insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34462206_34462207insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34462206_34462207insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34462206_34462207insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003315949.1:g.19585_19586dup, NW_003315949.1:g.19577_19586del, NW_003315949.1:g.19578_19586del, NW_003315949.1:g.19580_19586del, NW_003315949.1:g.19582_19586del, NW_003315949.1:g.19583_19586del, NW_003315949.1:g.19584_19586del, NW_003315949.1:g.19585_19586del, NW_003315949.1:g.19586del, NW_003315949.1:g.19586dup, NW_003315949.1:g.19584_19586dup, NW_003315949.1:g.19583_19586dup, NW_003315949.1:g.19582_19586dup, NW_003315949.1:g.19581_19586dup, NW_003315949.1:g.19580_19586dup, NW_003315949.1:g.19579_19586dup, NW_003315949.1:g.19578_19586dup, NW_003315949.1:g.19577_19586dup, NW_003315949.1:g.19576_19586dup, NW_003315949.1:g.19575_19586dup, NW_003315949.1:g.19574_19586dup, NW_003315949.1:g.19573_19586dup, NW_003315949.1:g.19572_19586dup, NW_003315949.1:g.19571_19586dup, NW_003315949.1:g.19570_19586dup, NW_003315949.1:g.19569_19586dup, NW_003315949.1:g.19568_19586dup, NW_003315949.1:g.19567_19586dup, NW_003315949.1:g.19586_19587insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003315949.1:g.19586_19587insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003315949.1:g.19586_19587insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003315949.1:g.19586_19587insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

    2.

    rs1491587486 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      TT>- [Show Flanks]
      Chromosome:
      17:36201132 (GRCh38)
      17:34528532 (GRCh37)
      Canonical SPDI:
      NC_000017.11:36201131:TT:
      Validated:
      by frequency,by alfa
      MAF:
      -=0./0 (ALFA)
      HGVS:

      3.

      rs1491551146 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        AG>- [Show Flanks]
        Chromosome:
        17:36188837 (GRCh38)
        17:34516213 (GRCh37)
        Canonical SPDI:
        NC_000017.11:36188836:AG:
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        -=0.00211/25 (ALFA)
        -=0.00035/5 (TOMMO)
        -=0.00249/235 (GnomAD)
        HGVS:

        4.

        rs1491515762 [Homo sapiens]
          Variant type:
          INS
          Alleles:
          ->C [Show Flanks]
          Chromosome:
          17:36139704 (GRCh38)
          17:34467090 (GRCh37)
          Canonical SPDI:
          NC_000017.11:36139704::C
          Gene:
          LOC101927369 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0.004131/49 (ALFA)
          C=0.000142/4 (TOMMO)
          C=0.008526/1150 (GnomAD)
          C=0.009994/64 (1000Genomes)
          HGVS:

          5.

          rs1491513130 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->C [Show Flanks]
            Chromosome:
            17:36101029 (GRCh38)
            17:34428424 (GRCh37)
            Canonical SPDI:
            NC_000017.11:36101029::C
            Validated:
            by frequency,by alfa
            MAF:
            C=0./0 (ALFA)
            HGVS:

            6.

            rs1491509707 [Homo sapiens]
              Variant type:
              INS
              Alleles:
              ->CA [Show Flanks]
              Chromosome:
              17:36180544 (GRCh38)
              17:34507921 (GRCh37)
              Canonical SPDI:
              NC_000017.11:36180544::CA
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              CA=0./0 (ALFA)
              CA=0.000004/1 (TOPMED)
              CA=0.000131/1 (GnomAD)
              HGVS:

              7.

              rs1491476686 has merged into rs771525653 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                Chromosome:
                17:36094227 (GRCh38)
                17:34421575 (GRCh37)
                Canonical SPDI:
                NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36094216:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AAAAAAAAAA=0./0 (ALFA)
                HGVS:
                NC_000017.11:g.36094227_36094244del, NC_000017.11:g.36094228_36094244del, NC_000017.11:g.36094229_36094244del, NC_000017.11:g.36094230_36094244del, NC_000017.11:g.36094231_36094244del, NC_000017.11:g.36094232_36094244del, NC_000017.11:g.36094233_36094244del, NC_000017.11:g.36094234_36094244del, NC_000017.11:g.36094235_36094244del, NC_000017.11:g.36094236_36094244del, NC_000017.11:g.36094237_36094244del, NC_000017.11:g.36094238_36094244del, NC_000017.11:g.36094239_36094244del, NC_000017.11:g.36094240_36094244del, NC_000017.11:g.36094241_36094244del, NC_000017.11:g.36094242_36094244del, NC_000017.11:g.36094243_36094244del, NC_000017.11:g.36094244del, NC_000017.11:g.36094244dup, NC_000017.11:g.36094243_36094244dup, NC_000017.11:g.36094242_36094244dup, NC_000017.11:g.36094241_36094244dup, NC_000017.11:g.36094240_36094244dup, NC_000017.11:g.36094239_36094244dup, NC_000017.11:g.36094238_36094244dup, NC_000017.11:g.36094237_36094244dup, NC_000017.11:g.36094236_36094244dup, NC_000017.11:g.36094235_36094244dup, NC_000017.11:g.36094234_36094244dup, NG_027730.2:g.909_926del, NG_027730.2:g.910_926del, NG_027730.2:g.911_926del, NG_027730.2:g.912_926del, NG_027730.2:g.913_926del, NG_027730.2:g.914_926del, NG_027730.2:g.915_926del, NG_027730.2:g.916_926del, NG_027730.2:g.917_926del, NG_027730.2:g.918_926del, NG_027730.2:g.919_926del, NG_027730.2:g.920_926del, NG_027730.2:g.921_926del, NG_027730.2:g.922_926del, NG_027730.2:g.923_926del, NG_027730.2:g.924_926del, NG_027730.2:g.925_926del, NG_027730.2:g.926del, NG_027730.2:g.926dup, NG_027730.2:g.925_926dup, NG_027730.2:g.924_926dup, NG_027730.2:g.923_926dup, NG_027730.2:g.922_926dup, NG_027730.2:g.921_926dup, NG_027730.2:g.920_926dup, NG_027730.2:g.919_926dup, NG_027730.2:g.918_926dup, NG_027730.2:g.917_926dup, NG_027730.2:g.916_926dup, NG_027730.1:g.933_942dup, NG_027730.1:g.935_942del, NG_027730.1:g.936_942del, NG_027730.1:g.937_942del, NG_027730.1:g.938_942del, NG_027730.1:g.939_942del, NG_027730.1:g.940_942del, NG_027730.1:g.941_942del, NG_027730.1:g.942del, NG_027730.1:g.942dup, NG_027730.1:g.941_942dup, NG_027730.1:g.940_942dup, NG_027730.1:g.939_942dup, NG_027730.1:g.938_942dup, NG_027730.1:g.937_942dup, NG_027730.1:g.936_942dup, NG_027730.1:g.935_942dup, NG_027730.1:g.934_942dup, NG_027730.1:g.932_942dup, NG_027730.1:g.931_942dup, NG_027730.1:g.930_942dup, NG_027730.1:g.929_942dup, NG_027730.1:g.928_942dup, NG_027730.1:g.927_942dup, NG_027730.1:g.926_942dup, NG_027730.1:g.925_942dup, NG_027730.1:g.942_943insTTTTTTTTTTTTTTTTTTT, NG_027730.1:g.942_943insTTTTTTTTTTTTTTTTTTTT, NG_027730.1:g.942_943insTTTTTTTTTTTTTTTTTTTTT, NT_187661.1:g.48324_48341del, NT_187661.1:g.48325_48341del, NT_187661.1:g.48326_48341del, NT_187661.1:g.48327_48341del, NT_187661.1:g.48328_48341del, NT_187661.1:g.48329_48341del, NT_187661.1:g.48330_48341del, NT_187661.1:g.48331_48341del, NT_187661.1:g.48332_48341del, NT_187661.1:g.48333_48341del, NT_187661.1:g.48334_48341del, NT_187661.1:g.48335_48341del, NT_187661.1:g.48336_48341del, NT_187661.1:g.48337_48341del, NT_187661.1:g.48338_48341del, NT_187661.1:g.48339_48341del, NT_187661.1:g.48340_48341del, NT_187661.1:g.48341del, NT_187661.1:g.48341dup, NT_187661.1:g.48340_48341dup, NT_187661.1:g.48339_48341dup, NT_187661.1:g.48338_48341dup, NT_187661.1:g.48337_48341dup, NT_187661.1:g.48336_48341dup, NT_187661.1:g.48335_48341dup, NT_187661.1:g.48334_48341dup, NT_187661.1:g.48333_48341dup, NT_187661.1:g.48332_48341dup, NT_187661.1:g.48331_48341dup, NT_187614.1:g.329101_329110dup, NT_187614.1:g.329103_329110del, NT_187614.1:g.329104_329110del, NT_187614.1:g.329105_329110del, NT_187614.1:g.329106_329110del, NT_187614.1:g.329107_329110del, NT_187614.1:g.329108_329110del, NT_187614.1:g.329109_329110del, NT_187614.1:g.329110del, NT_187614.1:g.329110dup, NT_187614.1:g.329109_329110dup, NT_187614.1:g.329108_329110dup, NT_187614.1:g.329107_329110dup, NT_187614.1:g.329106_329110dup, NT_187614.1:g.329105_329110dup, NT_187614.1:g.329104_329110dup, NT_187614.1:g.329103_329110dup, NT_187614.1:g.329102_329110dup, NT_187614.1:g.329100_329110dup, NT_187614.1:g.329099_329110dup, NT_187614.1:g.329098_329110dup, NT_187614.1:g.329097_329110dup, NT_187614.1:g.329096_329110dup, NT_187614.1:g.329095_329110dup, NT_187614.1:g.329094_329110dup, NT_187614.1:g.329093_329110dup, NT_187614.1:g.329110_329111insAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.329110_329111insAAAAAAAAAAAAAAAAAAAA, NT_187614.1:g.329110_329111insAAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34421573_34421582dup, NC_000017.10:g.34421575_34421582del, NC_000017.10:g.34421576_34421582del, NC_000017.10:g.34421577_34421582del, NC_000017.10:g.34421578_34421582del, NC_000017.10:g.34421579_34421582del, NC_000017.10:g.34421580_34421582del, NC_000017.10:g.34421581_34421582del, NC_000017.10:g.34421582del, NC_000017.10:g.34421582dup, NC_000017.10:g.34421581_34421582dup, NC_000017.10:g.34421580_34421582dup, NC_000017.10:g.34421579_34421582dup, NC_000017.10:g.34421578_34421582dup, NC_000017.10:g.34421577_34421582dup, NC_000017.10:g.34421576_34421582dup, NC_000017.10:g.34421575_34421582dup, NC_000017.10:g.34421574_34421582dup, NC_000017.10:g.34421572_34421582dup, NC_000017.10:g.34421571_34421582dup, NC_000017.10:g.34421570_34421582dup, NC_000017.10:g.34421569_34421582dup, NC_000017.10:g.34421568_34421582dup, NC_000017.10:g.34421567_34421582dup, NC_000017.10:g.34421566_34421582dup, NC_000017.10:g.34421565_34421582dup, NC_000017.10:g.34421582_34421583insAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34421582_34421583insAAAAAAAAAAAAAAAAAAAA, NC_000017.10:g.34421582_34421583insAAAAAAAAAAAAAAAAAAAAA

                8.

                rs1491466795 [Homo sapiens]
                  Variant type:
                  INS
                  Alleles:
                  ->G [Show Flanks]
                  Chromosome:
                  17:36241007 (GRCh38)
                  17:34670016 (GRCh37)
                  Canonical SPDI:
                  NC_000017.11:36241007::G
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.00011/3 (TOMMO)
                  HGVS:

                  9.

                  rs1491448663 has merged into rs1555653204 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT [Show Flanks]
                    Chromosome:
                    17:36101041 (GRCh38)
                    17:34428435 (GRCh37)
                    Canonical SPDI:
                    NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT,NC_000017.11:36101028:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    ATATATATATATAT=0./0 (ALFA)
                    HGVS:
                    NC_000017.11:g.36101029AT[6], NC_000017.11:g.36101029AT[7], NC_000017.11:g.36101029AT[8], NC_000017.11:g.36101029AT[10], NC_000017.11:g.36101029AT[11], NC_000017.11:g.36101029AT[12], NC_000017.11:g.36101029AT[14], NC_000017.11:g.36101029AT[15], NC_000017.11:g.36101029AT[17], NC_000017.11:g.36101029AT[21], NC_000017.11:g.36101029AT[22], NG_033066.2:g.2204AT[6], NG_033066.2:g.2204AT[7], NG_033066.2:g.2204AT[8], NG_033066.2:g.2204AT[10], NG_033066.2:g.2204AT[11], NG_033066.2:g.2204AT[12], NG_033066.2:g.2204AT[14], NG_033066.2:g.2204AT[15], NG_033066.2:g.2204AT[17], NG_033066.2:g.2204AT[21], NG_033066.2:g.2204AT[22], NT_187661.1:g.55126AT[6], NT_187661.1:g.55126AT[7], NT_187661.1:g.55126AT[8], NT_187661.1:g.55126AT[10], NT_187661.1:g.55126AT[11], NT_187661.1:g.55126AT[12], NT_187661.1:g.55126AT[14], NT_187661.1:g.55126AT[15], NT_187661.1:g.55126AT[17], NT_187661.1:g.55126AT[21], NT_187661.1:g.55126AT[22], NT_187614.1:g.335951AT[6], NT_187614.1:g.335951AT[7], NT_187614.1:g.335951AT[8], NT_187614.1:g.335951AT[10], NT_187614.1:g.335951AT[11], NT_187614.1:g.335951AT[12], NT_187614.1:g.335951AT[14], NT_187614.1:g.335951AT[15], NT_187614.1:g.335951AT[17], NT_187614.1:g.335951AT[21], NT_187614.1:g.335951AT[22], NC_000017.10:g.34428423AT[6], NC_000017.10:g.34428423AT[7], NC_000017.10:g.34428423AT[8], NC_000017.10:g.34428423AT[10], NC_000017.10:g.34428423AT[11], NC_000017.10:g.34428423AT[12], NC_000017.10:g.34428423AT[14], NC_000017.10:g.34428423AT[15], NC_000017.10:g.34428423AT[17], NC_000017.10:g.34428423AT[21], NC_000017.10:g.34428423AT[22]

                    10.

                    rs1491448556 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      ->A,AA,AAA,AAAAA [Show Flanks]
                      Chromosome:
                      17:36229428 (GRCh38)
                      17:34658436 (GRCh37)
                      Canonical SPDI:
                      NC_000017.11:36229428:AAA:AAAA,NC_000017.11:36229428:AAA:AAAAA,NC_000017.11:36229428:AAA:AAAAAA,NC_000017.11:36229428:AAA:AAAAAAAA
                      Gene:
                      LOC105371747 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAA=0./0 (ALFA)
                      HGVS:

                      11.

                      rs1491434189 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        TA>- [Show Flanks]
                        Chromosome:
                        17:36131459 (GRCh38)
                        17:34458841 (GRCh37)
                        Canonical SPDI:
                        NC_000017.11:36131458:TA:
                        Gene:
                        LOC101927369 (Varview)
                        Functional Consequence:
                        genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        -=0./0 (ALFA)
                        -=0.000049/5 (GnomAD)
                        HGVS:

                        12.

                        rs1491415032 [Homo sapiens]
                          Variant type:
                          SNV:
                          Alleles:
                          ->AAAA
                          Chromosome:
                          no mapping
                          Canonical SPDI:

                          13.

                          rs1491405311 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            CC>-,C [Show Flanks]
                            Chromosome:
                            17:36095561 (GRCh38)
                            17:34422903 (GRCh37)
                            Canonical SPDI:
                            NC_000017.11:36095559:CCC:C,NC_000017.11:36095559:CCC:CC
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            HGVS:

                            14.

                            rs1491383503 has merged into rs57582618 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              AAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
                              Chromosome:
                              17:36197360 (GRCh38)
                              17:34524759 (GRCh37)
                              Canonical SPDI:
                              NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:36197349:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
                              Gene:
                              CCL3L3 (Varview)
                              Functional Consequence:
                              upstream_transcript_variant,2KB_upstream_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              AAAAAAAAAAAAAAAA=0./0 (ALFA)
                              HGVS:
                              NC_000017.11:g.36197360_36197367del, NC_000017.11:g.36197364_36197367del, NC_000017.11:g.36197365_36197367del, NC_000017.11:g.36197366_36197367del, NC_000017.11:g.36197367del, NC_000017.11:g.36197367dup, NC_000017.11:g.36197366_36197367dup, NC_000017.11:g.36197365_36197367dup, NC_000017.11:g.36197364_36197367dup, NC_000017.11:g.36197363_36197367dup, NC_000017.11:g.36197359_36197367dup, NC_000017.11:g.36197358_36197367dup, NG_023325.2:g.4401_4408del, NG_023325.2:g.4405_4408del, NG_023325.2:g.4406_4408del, NG_023325.2:g.4407_4408del, NG_023325.2:g.4408del, NG_023325.2:g.4408dup, NG_023325.2:g.4407_4408dup, NG_023325.2:g.4406_4408dup, NG_023325.2:g.4405_4408dup, NG_023325.2:g.4404_4408dup, NG_023325.2:g.4400_4408dup, NG_023325.2:g.4399_4408dup, NG_023325.1:g.4392_4399del, NG_023325.1:g.4396_4399del, NG_023325.1:g.4397_4399del, NG_023325.1:g.4398_4399del, NG_023325.1:g.4399del, NG_023325.1:g.4399dup, NG_023325.1:g.4398_4399dup, NG_023325.1:g.4397_4399dup, NG_023325.1:g.4396_4399dup, NG_023325.1:g.4395_4399dup, NG_023325.1:g.4391_4399dup, NG_023325.1:g.4390_4399dup, NG_026174.1:g.35881_35888del, NG_026174.1:g.35885_35888del, NG_026174.1:g.35886_35888del, NG_026174.1:g.35887_35888del, NG_026174.1:g.35888del, NG_026174.1:g.35888dup, NG_026174.1:g.35887_35888dup, NG_026174.1:g.35886_35888dup, NG_026174.1:g.35885_35888dup, NG_026174.1:g.35884_35888dup, NG_026174.1:g.35880_35888dup, NG_026174.1:g.35879_35888dup, NT_187661.1:g.151495_151502del, NT_187661.1:g.151499_151502del, NT_187661.1:g.151500_151502del, NT_187661.1:g.151501_151502del, NT_187661.1:g.151502del, NT_187661.1:g.151502dup, NT_187661.1:g.151501_151502dup, NT_187661.1:g.151500_151502dup, NT_187661.1:g.151499_151502dup, NT_187661.1:g.151498_151502dup, NT_187661.1:g.151494_151502dup, NT_187661.1:g.151493_151502dup, NC_000017.10:g.34524760_34524767del, NC_000017.10:g.34524764_34524767del, NC_000017.10:g.34524765_34524767del, NC_000017.10:g.34524766_34524767del, NC_000017.10:g.34524767del, NC_000017.10:g.34524767dup, NC_000017.10:g.34524766_34524767dup, NC_000017.10:g.34524765_34524767dup, NC_000017.10:g.34524764_34524767dup, NC_000017.10:g.34524763_34524767dup, NC_000017.10:g.34524759_34524767dup, NC_000017.10:g.34524758_34524767dup, NT_187614.1:g.432264_432271del, NT_187614.1:g.432268_432271del, NT_187614.1:g.432269_432271del, NT_187614.1:g.432270_432271del, NT_187614.1:g.432271del, NT_187614.1:g.432271dup, NT_187614.1:g.432270_432271dup, NT_187614.1:g.432269_432271dup, NT_187614.1:g.432268_432271dup, NT_187614.1:g.432267_432271dup, NT_187614.1:g.432263_432271dup, NT_187614.1:g.432262_432271dup, NW_003315949.1:g.82116_82123del, NW_003315949.1:g.82120_82123del, NW_003315949.1:g.82121_82123del, NW_003315949.1:g.82122_82123del, NW_003315949.1:g.82123del, NW_003315949.1:g.82123dup, NW_003315949.1:g.82122_82123dup, NW_003315949.1:g.82121_82123dup, NW_003315949.1:g.82120_82123dup, NW_003315949.1:g.82119_82123dup, NW_003315949.1:g.82115_82123dup, NW_003315949.1:g.82114_82123dup

                              15.

                              rs1491379627 has merged into rs61015482 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
                                Chromosome:
                                17:36134837 (GRCh38)
                                17:34462217 (GRCh37)
                                Canonical SPDI:
                                NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000017.11:36134827:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
                                Gene:
                                LOC101927369 (Varview), LOC107985055 (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,downstream_transcript_variant,upstream_transcript_variant,intron_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                TTTTTTTTTTT=0./0 (ALFA)
                                -=0.000004/1 (TOPMED)
                                -=0.174061/102 (NorthernSweden)
                                HGVS:
                                NC_000017.11:g.36134837_36134842del, NC_000017.11:g.36134839_36134842del, NC_000017.11:g.36134840_36134842del, NC_000017.11:g.36134841_36134842del, NC_000017.11:g.36134842del, NC_000017.11:g.36134842dup, NC_000017.11:g.36134841_36134842dup, NT_187614.1:g.369745_369750del, NT_187614.1:g.369747_369750del, NT_187614.1:g.369748_369750del, NT_187614.1:g.369749_369750del, NT_187614.1:g.369750del, NT_187614.1:g.369750dup, NT_187614.1:g.369749_369750dup, NC_000017.10:g.34462217_34462222del, NC_000017.10:g.34462219_34462222del, NC_000017.10:g.34462220_34462222del, NC_000017.10:g.34462221_34462222del, NC_000017.10:g.34462222del, NC_000017.10:g.34462222dup, NC_000017.10:g.34462221_34462222dup, NT_187661.1:g.88934_88939del, NT_187661.1:g.88936_88939del, NT_187661.1:g.88937_88939del, NT_187661.1:g.88938_88939del, NT_187661.1:g.88939del, NT_187661.1:g.88939dup, NT_187661.1:g.88938_88939dup, NW_003315949.1:g.19597_19602del, NW_003315949.1:g.19599_19602del, NW_003315949.1:g.19600_19602del, NW_003315949.1:g.19601_19602del, NW_003315949.1:g.19602del, NW_003315949.1:g.19602dup, NW_003315949.1:g.19601_19602dup

                                16.

                                rs1491375840 has merged into rs57793857 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  TGTGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
                                  Chromosome:
                                  17:36086290 (GRCh38)
                                  17:34413639 (GRCh37)
                                  Canonical SPDI:
                                  NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000017.11:36086269:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TGTGTGTGTGTGTGTGTGTGTG=0./0 (ALFA)
                                  HGVS:
                                  NC_000017.11:g.36086270TG[10], NC_000017.11:g.36086270TG[11], NC_000017.11:g.36086270TG[12], NC_000017.11:g.36086270TG[13], NC_000017.11:g.36086270TG[14], NC_000017.11:g.36086270TG[15], NC_000017.11:g.36086270TG[16], NC_000017.11:g.36086270TG[17], NC_000017.11:g.36086270TG[19], NC_000017.11:g.36086270TG[20], NC_000017.11:g.36086270TG[21], NC_000017.11:g.36086270TG[22], NC_000017.11:g.36086270TG[23], NC_000017.11:g.36086270TG[24], NC_000017.11:g.36086270TG[25], NC_000017.11:g.36086270TG[26], NC_000017.11:g.36086270TG[27], NG_027730.2:g.8838CA[10], NG_027730.2:g.8838CA[11], NG_027730.2:g.8838CA[12], NG_027730.2:g.8838CA[13], NG_027730.2:g.8838CA[14], NG_027730.2:g.8838CA[15], NG_027730.2:g.8838CA[16], NG_027730.2:g.8838CA[17], NG_027730.2:g.8838CA[19], NG_027730.2:g.8838CA[20], NG_027730.2:g.8838CA[21], NG_027730.2:g.8838CA[22], NG_027730.2:g.8838CA[23], NG_027730.2:g.8838CA[24], NG_027730.2:g.8838CA[25], NG_027730.2:g.8838CA[26], NG_027730.2:g.8838CA[27], NG_027730.1:g.8855CA[18], NG_027730.1:g.8855CA[10], NG_027730.1:g.8855CA[11], NG_027730.1:g.8855CA[12], NG_027730.1:g.8855CA[13], NG_027730.1:g.8855CA[14], NG_027730.1:g.8855CA[15], NG_027730.1:g.8855CA[16], NG_027730.1:g.8855CA[19], NG_027730.1:g.8855CA[20], NG_027730.1:g.8855CA[21], NG_027730.1:g.8855CA[22], NG_027730.1:g.8855CA[23], NG_027730.1:g.8855CA[24], NG_027730.1:g.8855CA[25], NG_027730.1:g.8855CA[26], NG_027730.1:g.8855CA[27], NT_187661.1:g.40367TG[10], NT_187661.1:g.40367TG[11], NT_187661.1:g.40367TG[12], NT_187661.1:g.40367TG[13], NT_187661.1:g.40367TG[14], NT_187661.1:g.40367TG[15], NT_187661.1:g.40367TG[16], NT_187661.1:g.40367TG[17], NT_187661.1:g.40367TG[19], NT_187661.1:g.40367TG[20], NT_187661.1:g.40367TG[21], NT_187661.1:g.40367TG[22], NT_187661.1:g.40367TG[23], NT_187661.1:g.40367TG[24], NT_187661.1:g.40367TG[25], NT_187661.1:g.40367TG[26], NT_187661.1:g.40367TG[27], NT_187614.1:g.321147TG[18], NT_187614.1:g.321147TG[10], NT_187614.1:g.321147TG[11], NT_187614.1:g.321147TG[12], NT_187614.1:g.321147TG[13], NT_187614.1:g.321147TG[14], NT_187614.1:g.321147TG[15], NT_187614.1:g.321147TG[16], NT_187614.1:g.321147TG[19], NT_187614.1:g.321147TG[20], NT_187614.1:g.321147TG[21], NT_187614.1:g.321147TG[22], NT_187614.1:g.321147TG[23], NT_187614.1:g.321147TG[24], NT_187614.1:g.321147TG[25], NT_187614.1:g.321147TG[26], NT_187614.1:g.321147TG[27], NC_000017.10:g.34413619TG[18], NC_000017.10:g.34413619TG[10], NC_000017.10:g.34413619TG[11], NC_000017.10:g.34413619TG[12], NC_000017.10:g.34413619TG[13], NC_000017.10:g.34413619TG[14], NC_000017.10:g.34413619TG[15], NC_000017.10:g.34413619TG[16], NC_000017.10:g.34413619TG[19], NC_000017.10:g.34413619TG[20], NC_000017.10:g.34413619TG[21], NC_000017.10:g.34413619TG[22], NC_000017.10:g.34413619TG[23], NC_000017.10:g.34413619TG[24], NC_000017.10:g.34413619TG[25], NC_000017.10:g.34413619TG[26], NC_000017.10:g.34413619TG[27]

                                  17.

                                  rs1491364879 has merged into rs35673879 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    CACACACA>-,CA,CACA,CACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA [Show Flanks]
                                    Chromosome:
                                    17:36093859 (GRCh38)
                                    17:34421207 (GRCh37)
                                    Canonical SPDI:
                                    NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000017.11:36093847:ACACACACACACACACACA:ACACACACACACACACACACACACACACACACA
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    ACACACACACACA=0./0 (ALFA)
                                    AC=0.18167/109 (NorthernSweden)
                                    HGVS:
                                    NC_000017.11:g.36093849CA[5], NC_000017.11:g.36093849CA[6], NC_000017.11:g.36093849CA[7], NC_000017.11:g.36093849CA[8], NC_000017.11:g.36093849CA[10], NC_000017.11:g.36093849CA[11], NC_000017.11:g.36093849CA[12], NC_000017.11:g.36093849CA[15], NC_000017.11:g.36093849CA[16], NG_027730.2:g.1278GT[5], NG_027730.2:g.1278GT[6], NG_027730.2:g.1278GT[7], NG_027730.2:g.1278GT[8], NG_027730.2:g.1278GT[10], NG_027730.2:g.1278GT[11], NG_027730.2:g.1278GT[12], NG_027730.2:g.1278GT[15], NG_027730.2:g.1278GT[16], NG_027730.1:g.1294GT[5], NG_027730.1:g.1294GT[6], NG_027730.1:g.1294GT[7], NG_027730.1:g.1294GT[8], NG_027730.1:g.1294GT[10], NG_027730.1:g.1294GT[11], NG_027730.1:g.1294GT[12], NG_027730.1:g.1294GT[15], NG_027730.1:g.1294GT[16], NT_187661.1:g.47946CA[5], NT_187661.1:g.47946CA[6], NT_187661.1:g.47946CA[7], NT_187661.1:g.47946CA[8], NT_187661.1:g.47946CA[10], NT_187661.1:g.47946CA[11], NT_187661.1:g.47946CA[12], NT_187661.1:g.47946CA[15], NT_187661.1:g.47946CA[16], NT_187614.1:g.328725CA[5], NT_187614.1:g.328725CA[6], NT_187614.1:g.328725CA[7], NT_187614.1:g.328725CA[8], NT_187614.1:g.328725CA[10], NT_187614.1:g.328725CA[11], NT_187614.1:g.328725CA[12], NT_187614.1:g.328725CA[15], NT_187614.1:g.328725CA[16], NC_000017.10:g.34421197CA[5], NC_000017.10:g.34421197CA[6], NC_000017.10:g.34421197CA[7], NC_000017.10:g.34421197CA[8], NC_000017.10:g.34421197CA[10], NC_000017.10:g.34421197CA[11], NC_000017.10:g.34421197CA[12], NC_000017.10:g.34421197CA[15], NC_000017.10:g.34421197CA[16]

                                    18.

                                    rs1491355654 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      T>-,TT,TTCTTT,TTCTTTCTTT,TTCTTTCTTTCTTT,TTCTTTCTTTCTTTCTTT,TTCTTTCTTTCTTTCTTTCTTT,TTCTTTCTTTCTTTCTTTCTTTCTTT [Show Flanks]
                                      Chromosome:
                                      17:36095643 (GRCh38)
                                      17:34423012 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:36095642:TT:T,NC_000017.11:36095642:TT:TTT,NC_000017.11:36095642:TT:TTTCTTT,NC_000017.11:36095642:TT:TTTCTTTCTTT,NC_000017.11:36095642:TT:TTTCTTTCTTTCTTT,NC_000017.11:36095642:TT:TTTCTTTCTTTCTTTCTTT,NC_000017.11:36095642:TT:TTTCTTTCTTTCTTTCTTTCTTT,NC_000017.11:36095642:TT:TTTCTTTCTTTCTTTCTTTCTTTCTTT
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TTT=0./0 (ALFA)
                                      HGVS:
                                      NC_000017.11:g.36095644del, NC_000017.11:g.36095644dup, NC_000017.11:g.36095644_36095645insTCTTT, NC_000017.11:g.36095643_36095644TTTC[2]TTT[1], NC_000017.11:g.36095643_36095644TTTC[3]TTT[1], NC_000017.11:g.36095643_36095644TTTC[4]TTT[1], NC_000017.11:g.36095643_36095644TTTC[5]TTT[1], NC_000017.11:g.36095643_36095644TTTC[6]TTT[1], NT_187614.1:g.330566del, NT_187614.1:g.330566dup, NT_187614.1:g.330562_330566dup, NT_187614.1:g.330558_330566dup, NT_187614.1:g.330554_330566dup, NT_187614.1:g.330550_330566dup, NT_187614.1:g.330546_330566dup, NT_187614.1:g.330542_330566dup, NC_000017.10:g.34423038del, NC_000017.10:g.34423038dup, NC_000017.10:g.34423034_34423038dup, NC_000017.10:g.34423030_34423038dup, NC_000017.10:g.34423026_34423038dup, NC_000017.10:g.34423022_34423038dup, NC_000017.10:g.34423018_34423038dup, NC_000017.10:g.34423014_34423038dup, NT_187661.1:g.49741del, NT_187661.1:g.49741dup, NT_187661.1:g.49741_49742insTCTTT, NT_187661.1:g.49740_49741TTTC[2]TTT[1], NT_187661.1:g.49740_49741TTTC[3]TTT[1], NT_187661.1:g.49740_49741TTTC[4]TTT[1], NT_187661.1:g.49740_49741TTTC[5]TTT[1], NT_187661.1:g.49740_49741TTTC[6]TTT[1]

                                      19.

                                      rs1491326149 [Homo sapiens]
                                        Variant type:
                                        SNV:
                                        Alleles:
                                        CTCC>-
                                        Chromosome:
                                        no mapping
                                        Canonical SPDI:

                                        20.

                                        rs1491318125 [Homo sapiens]
                                          Variant type:
                                          INS
                                          Alleles:
                                          ->C [Show Flanks]
                                          Chromosome:
                                          17:36148707 (GRCh38)
                                          17:34476090 (GRCh37)
                                          Canonical SPDI:
                                          NC_000017.11:36148707::C
                                          Gene:
                                          LOC101927369 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000064/9 (GnomAD)
                                          HGVS:

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