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Items: 1 to 20 of 8235

1.

rs1491588300 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->AT [Show Flanks]
    Chromosome:
    10:123683033 (GRCh38)
    10:125442550 (GRCh37)
    Canonical SPDI:
    NC_000010.11:123683033::AT
    Gene:
    GPR26 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AT=0./0 (ALFA)
    AT=0.000185/49 (TOPMED)
    AT=0.000194/27 (GnomAD)
    HGVS:

    2.

    rs1491525098 [Homo sapiens]
      Variant type:
      INS
      Alleles:
      ->TG,TGG,TTG [Show Flanks]
      Chromosome:
      10:123680827 (GRCh38)
      10:125440344 (GRCh37)
      Canonical SPDI:
      NC_000010.11:123680827::TG,NC_000010.11:123680827::TGG,NC_000010.11:123680827::TTG
      Gene:
      GPR26 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TG=0.00008/1 (ALFA)
      TG=0.00036/5 (TOMMO)
      TG=0.0008/72 (GnomAD)
      HGVS:

      3.

      rs1491450343 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        GT>- [Show Flanks]
        Chromosome:
        10:123680838 (GRCh38)
        10:125440354 (GRCh37)
        Canonical SPDI:
        NC_000010.11:123680837:GT:
        Gene:
        GPR26 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        -=0./0 (ALFA)
        HGVS:

        4.

        rs1491402933 has merged into rs57869785 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          GTGT>-,GT,GTGTGT,GTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGT,GTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTACATGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTCCGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTTCGTGTGTGTGTGTGTGTGTGT [Show Flanks]
          Chromosome:
          10:123675814 (GRCh38)
          10:125435330 (GRCh37)
          Canonical SPDI:
          NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACATGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCCGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:123675798:TGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCGTGTGTGTGTGTGTGTGTGT
          Gene:
          GPR26 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TGTGTGTGTGTGTGTGT=0./0 (ALFA)
          HGVS:
          NC_000010.11:g.123675800GT[7], NC_000010.11:g.123675800GT[8], NC_000010.11:g.123675800GT[10], NC_000010.11:g.123675799_123675817TG[10]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[11], NC_000010.11:g.123675799_123675817TG[11]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[11]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TGTGTGTGTGTGTGTGTGTGTGTACG[2]TG[10]T[1], NC_000010.11:g.123675799_123675817TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[12]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[12], NC_000010.11:g.123675799_123675817TG[12]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[12]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[13], NC_000010.11:g.123675799_123675817TG[13]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[13]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[13]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[14], NC_000010.11:g.123675799_123675817TG[14]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[14]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[14]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[14]TATGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[15], NC_000010.11:g.123675799_123675817TG[15]TACATGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[15]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[15]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[15]TCCGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[16]CGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[16]CGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[16]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[16], NC_000010.11:g.123675799_123675817TG[16]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[16]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[16]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[17]CGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[17], NC_000010.11:g.123675799_123675817TG[17]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[18]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675799_123675817TG[18]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[19], NC_000010.11:g.123675799_123675817TG[20]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800GT[21], NC_000010.11:g.123675800GT[23], NC_000010.11:g.123675799_123675817TG[15]TTCGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[7], NC_000010.10:g.125435316GT[8], NC_000010.10:g.125435316GT[10], NC_000010.10:g.125435315_125435333TG[10]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[11], NC_000010.10:g.125435315_125435333TG[11]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[11]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TGTGTGTGTGTGTGTGTGTGTGTACG[2]TG[10]T[1], NC_000010.10:g.125435315_125435333TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[12]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[12], NC_000010.10:g.125435315_125435333TG[12]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[12]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[13], NC_000010.10:g.125435315_125435333TG[13]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[13]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[13]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[14], NC_000010.10:g.125435315_125435333TG[14]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[14]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[14]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[14]TATGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[15], NC_000010.10:g.125435315_125435333TG[15]TACATGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[15]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[15]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[15]TCCGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[16]CGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[16]CGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[16]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[16], NC_000010.10:g.125435315_125435333TG[16]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[16]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[16]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[17]CGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[17], NC_000010.10:g.125435315_125435333TG[17]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[18]TACGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435315_125435333TG[18]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[19], NC_000010.10:g.125435315_125435333TG[20]TACGTGTGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316GT[21], NC_000010.10:g.125435316GT[23], NC_000010.10:g.125435315_125435333TG[15]TTCGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[7], NG_051571.1:g.14446GT[8], NG_051571.1:g.14446GT[10], NG_051571.1:g.14445_14463TG[10]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[10]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[11], NG_051571.1:g.14445_14463TG[11]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[11]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TGTGTGTGTGTGTGTGTGTGTGTACG[2]TG[10]T[1], NG_051571.1:g.14445_14463TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[11]TACGTGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[12]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[12], NG_051571.1:g.14445_14463TG[12]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[12]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[13], NG_051571.1:g.14445_14463TG[13]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[13]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[13]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[14], NG_051571.1:g.14445_14463TG[14]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[14]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[14]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[14]TATGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[15], NG_051571.1:g.14445_14463TG[15]TACATGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[15]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[15]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[15]TACGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[15]TCCGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[16]CGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[16]CGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[16]CGTGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[16], NG_051571.1:g.14445_14463TG[16]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[16]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[16]TACGTGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[17]CGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[17], NG_051571.1:g.14445_14463TG[17]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[18]TACGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14445_14463TG[18]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[19], NG_051571.1:g.14445_14463TG[20]TACGTGTGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446GT[21], NG_051571.1:g.14446GT[23], NG_051571.1:g.14445_14463TG[15]TTCGTGTGTGTGTGTGTGTGTGT[1]

          5.

          rs1491375832 has merged into rs1450040013 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            GT>- [Show Flanks]
            Chromosome:
            10:123680820 (GRCh38)
            10:125440336 (GRCh37)
            Canonical SPDI:
            NC_000010.11:123680818:TGT:T
            Gene:
            GPR26 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0.00042/5 (ALFA)
            -=0.02269/1566 (GnomAD)
            -=0.03014/193 (1000Genomes)
            -=0.05776/96 (Korea1K)
            -=0.05843/796 (TOMMO)
            HGVS:

            6.

            rs1491279952 [Homo sapiens]
              Variant type:
              DEL
              Alleles:
              CG>- [Show Flanks]
              Chromosome:
              10:123683033 (GRCh38)
              10:125442549 (GRCh37)
              Canonical SPDI:
              NC_000010.11:123683032:CG:
              Gene:
              GPR26 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              -=0./0 (ALFA)
              HGVS:

              7.

              rs1491279178 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->C [Show Flanks]
                Chromosome:
                10:123689266 (GRCh38)
                10:125448783 (GRCh37)
                Canonical SPDI:
                NC_000010.11:123689266:C:CC
                Gene:
                GPR26 (Varview)
                Functional Consequence:
                3_prime_UTR_variant
                Validated:
                by frequency,by alfa
                MAF:
                CC=0./0 (ALFA)
                C=0.000076/10 (GnomAD)
                HGVS:

                8.

                rs1491276587 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  ->GTGTACGTGTGTGTGTGTGTGTGT,GTGTGTGTACGTGTGTGTGTGTGTGTGT,GTGTGTGTGTACGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTACGTGAGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTACGTGGGTGTGTGTGTGTGTGTGT [Show Flanks]
                  Chromosome:
                  10:123675799 (GRCh38)
                  10:125435316 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGAGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT,NC_000010.11:123675799:GTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGGGTGTGTGTGTGTGTGTGT
                  Gene:
                  GPR26 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  GTGTGTGTGTGTGTGTGTGTGTACGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
                  GTGTGTGTGTGTGTGTGTGTGTAC=0.000004/1 (TOPMED)
                  GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAC=0.001976/3 (Korea1K)
                  HGVS:
                  NC_000010.11:g.123675800_123675817GT[11]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[13]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[14]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[15]ACGTGAGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[15]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[16]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.11:g.123675800_123675817GT[20]ACGTGGGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[11]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[13]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[14]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[15]ACGTGAGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[15]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[16]ACGTGTGTGTGTGTGTGTGT[1], NC_000010.10:g.125435316_125435333GT[20]ACGTGGGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[11]ACGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[13]ACGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[14]ACGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[15]ACGTGAGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[15]ACGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[16]ACGTGTGTGTGTGTGTGTGT[1], NG_051571.1:g.14446_14463GT[20]ACGTGGGTGTGTGTGTGTGTGTGT[1]

                  9.

                  rs1491250661 has merged into rs1490606651 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    GAGA>-,GA,GAGAGA [Show Flanks]
                    Chromosome:
                    10:123675868 (GRCh38)
                    10:125435384 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGA,NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGAGA,NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA
                    Gene:
                    GPR26 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AGAGAGAGAGAGA=0./0 (ALFA)
                    AG=0.0003/5 (TOMMO)
                    HGVS:

                    10.

                    rs1491075380 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AG>- [Show Flanks]
                      Chromosome:
                      10:123683051 (GRCh38)
                      10:125442567 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:123683049:GAG:G
                      Gene:
                      GPR26 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      G=0./0 (ALFA)
                      -=0.000011/3 (TOPMED)
                      -=0.000035/1 (TOMMO)
                      HGVS:

                      11.

                      rs1491059297 [Homo sapiens]
                        Variant type:
                        SNV:
                        Alleles:
                        TA>-
                        Chromosome:
                        no mapping
                        Canonical SPDI:

                        12.

                        rs1490957406 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          A>- [Show Flanks]
                          Chromosome:
                          10:123695234 (GRCh38)
                          10:125454750 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:123695233:AAA:AA
                          Gene:
                          GPR26 (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          AA=0.000071/1 (ALFA)
                          -=0.000004/1 (TOPMED)
                          -=0.000007/1 (GnomAD)
                          HGVS:

                          13.

                          rs1490814558 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            10:123668136 (GRCh38)
                            10:125427652 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:123668135:G:A
                            Gene:
                            GPR26 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1490670383 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              ->C [Show Flanks]
                              Chromosome:
                              10:123692535 (GRCh38)
                              10:125452052 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:123692535:C:CC
                              Gene:
                              GPR26 (Varview)
                              Functional Consequence:
                              3_prime_UTR_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              CC=0./0 (ALFA)
                              C=0.000007/1 (GnomAD)
                              C=0.000008/2 (TOPMED)
                              HGVS:

                              15.

                              rs1490606651 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                GAGA>-,GA,GAGAGA [Show Flanks]
                                Chromosome:
                                10:123675868 (GRCh38)
                                10:125435384 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGA,NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGAGA,NC_000010.11:123675856:AGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA
                                Gene:
                                GPR26 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                AGAGAGAGAGAGA=0./0 (ALFA)
                                AG=0.0003/5 (TOMMO)
                                HGVS:

                                16.

                                rs1490603586 [Homo sapiens]
                                  Variant type:
                                  DEL
                                  Alleles:
                                  T>- [Show Flanks]
                                  Chromosome:
                                  10:123691381 (GRCh38)
                                  10:125450897 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:123691380:T:
                                  Gene:
                                  GPR26 (Varview)
                                  Functional Consequence:
                                  3_prime_UTR_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  -=0./0 (ALFA)
                                  -=0.000007/1 (GnomAD)
                                  -=0.000019/5 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490337136 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    10:123682554 (GRCh38)
                                    10:125442070 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:123682553:C:T
                                    Gene:
                                    GPR26 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0.000071/1 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490314774 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      10:123667693 (GRCh38)
                                      10:125427209 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:123667692:C:T
                                      Gene:
                                      GPR26 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000021/3 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1490226046 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        10:123688686 (GRCh38)
                                        10:125448202 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:123688685:G:A
                                        Gene:
                                        GPR26 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0.000071/1 (ALFA)
                                        A=0.000015/4 (TOPMED)
                                        A=0.000021/3 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1490179508 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          10:123691970 (GRCh38)
                                          10:125451486 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:123691969:T:C
                                          Gene:
                                          GPR26 (Varview)
                                          Functional Consequence:
                                          3_prime_UTR_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          C=0.000007/1 (GnomAD)
                                          HGVS:

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