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Items: 1 to 20 of 1000

1.

rs1491584355 has merged into rs34126564 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
    Chromosome:
    3:51599757 (GRCh38)
    3:51633773 (GRCh37)
    Canonical SPDI:
    NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:51599745:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
    Gene:
    RAD54L2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAAAAAAA=0./0 (ALFA)
    -=0.0719/277 (ALSPAC)
    -=0.4497/2252 (1000Genomes)
    HGVS:

    2.

    rs1491564089 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      GT>- [Show Flanks]
      Chromosome:
      3:51592054 (GRCh38)
      3:51626070 (GRCh37)
      Canonical SPDI:
      NC_000003.12:51592051:GTGT:GT
      Gene:
      RAD54L2 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      GTGT=0./0 (ALFA)
      -=0.00133/22 (TOMMO)
      HGVS:

      3.

      rs1491555137 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->T [Show Flanks]
        Chromosome:
        3:51557854 (GRCh38)
        3:51591871 (GRCh37)
        Canonical SPDI:
        NC_000003.12:51557854::T
        Gene:
        RAD54L2 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        T=0./0 (ALFA)
        T=0.000007/1 (GnomAD)
        HGVS:

        4.

        rs1491551925 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->TTT [Show Flanks]
          Chromosome:
          3:51592052 (GRCh38)
          3:51626069 (GRCh37)
          Canonical SPDI:
          NC_000003.12:51592052:T:TTTT
          Gene:
          RAD54L2 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          TTTT=0./0 (ALFA)
          TTT=0.00004/1 (TOMMO)
          HGVS:

          5.

          rs1491543352 has merged into rs34235841 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
            Chromosome:
            3:51663605 (GRCh38)
            3:51697621 (GRCh37)
            Canonical SPDI:
            NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:51663594:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
            Gene:
            RAD54L2 (Varview)
            Functional Consequence:
            3_prime_UTR_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            AAAAAAAAAA=0./0 (ALFA)
            A=0.498/2494 (1000Genomes)
            HGVS:
            NC_000003.12:g.51663605_51663618del, NC_000003.12:g.51663606_51663618del, NC_000003.12:g.51663607_51663618del, NC_000003.12:g.51663608_51663618del, NC_000003.12:g.51663609_51663618del, NC_000003.12:g.51663611_51663618del, NC_000003.12:g.51663612_51663618del, NC_000003.12:g.51663613_51663618del, NC_000003.12:g.51663614_51663618del, NC_000003.12:g.51663615_51663618del, NC_000003.12:g.51663616_51663618del, NC_000003.12:g.51663617_51663618del, NC_000003.12:g.51663618del, NC_000003.12:g.51663618dup, NC_000003.12:g.51663617_51663618dup, NC_000003.12:g.51663616_51663618dup, NC_000003.12:g.51663615_51663618dup, NC_000003.12:g.51663612_51663618dup, NC_000003.12:g.51663611_51663618dup, NC_000003.12:g.51663610_51663618dup, NC_000003.12:g.51663609_51663618dup, NC_000003.12:g.51663608_51663618dup, NC_000003.12:g.51663606_51663618dup, NC_000003.12:g.51663597_51663618dup, NC_000003.12:g.51663618_51663619insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.51697621_51697634del, NC_000003.11:g.51697622_51697634del, NC_000003.11:g.51697623_51697634del, NC_000003.11:g.51697624_51697634del, NC_000003.11:g.51697625_51697634del, NC_000003.11:g.51697627_51697634del, NC_000003.11:g.51697628_51697634del, NC_000003.11:g.51697629_51697634del, NC_000003.11:g.51697630_51697634del, NC_000003.11:g.51697631_51697634del, NC_000003.11:g.51697632_51697634del, NC_000003.11:g.51697633_51697634del, NC_000003.11:g.51697634del, NC_000003.11:g.51697634dup, NC_000003.11:g.51697633_51697634dup, NC_000003.11:g.51697632_51697634dup, NC_000003.11:g.51697631_51697634dup, NC_000003.11:g.51697628_51697634dup, NC_000003.11:g.51697627_51697634dup, NC_000003.11:g.51697626_51697634dup, NC_000003.11:g.51697625_51697634dup, NC_000003.11:g.51697624_51697634dup, NC_000003.11:g.51697622_51697634dup, NC_000003.11:g.51697613_51697634dup, NC_000003.11:g.51697634_51697635insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_015106.4:c.*185_*198del, NM_015106.4:c.*186_*198del, NM_015106.4:c.*187_*198del, NM_015106.4:c.*188_*198del, NM_015106.4:c.*189_*198del, NM_015106.4:c.*191_*198del, NM_015106.4:c.*192_*198del, NM_015106.4:c.*193_*198del, NM_015106.4:c.*194_*198del, NM_015106.4:c.*195_*198del, NM_015106.4:c.*196_*198del, NM_015106.4:c.*197_*198del, NM_015106.4:c.*198del, NM_015106.4:c.*198dup, NM_015106.4:c.*197_*198dup, NM_015106.4:c.*196_*198dup, NM_015106.4:c.*195_*198dup, NM_015106.4:c.*192_*198dup, NM_015106.4:c.*191_*198dup, NM_015106.4:c.*190_*198dup, NM_015106.4:c.*189_*198dup, NM_015106.4:c.*188_*198dup, NM_015106.4:c.*186_*198dup, NM_015106.4:c.*177_*198dup, NM_015106.4:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_015106.3:c.*185_*198del, NM_015106.3:c.*186_*198del, NM_015106.3:c.*187_*198del, NM_015106.3:c.*188_*198del, NM_015106.3:c.*189_*198del, NM_015106.3:c.*191_*198del, NM_015106.3:c.*192_*198del, NM_015106.3:c.*193_*198del, NM_015106.3:c.*194_*198del, NM_015106.3:c.*195_*198del, NM_015106.3:c.*196_*198del, NM_015106.3:c.*197_*198del, NM_015106.3:c.*198del, NM_015106.3:c.*198dup, NM_015106.3:c.*197_*198dup, NM_015106.3:c.*196_*198dup, NM_015106.3:c.*195_*198dup, NM_015106.3:c.*192_*198dup, NM_015106.3:c.*191_*198dup, NM_015106.3:c.*190_*198dup, NM_015106.3:c.*189_*198dup, NM_015106.3:c.*188_*198dup, NM_015106.3:c.*186_*198dup, NM_015106.3:c.*177_*198dup, NM_015106.3:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_015106.2:c.*189_*202del, NM_015106.2:c.*190_*202del, NM_015106.2:c.*191_*202del, NM_015106.2:c.*192_*202del, NM_015106.2:c.*193_*202del, NM_015106.2:c.*195_*202del, NM_015106.2:c.*196_*202del, NM_015106.2:c.*197_*202del, NM_015106.2:c.*198_*202del, NM_015106.2:c.*199_*202del, NM_015106.2:c.*200_*202del, NM_015106.2:c.*201_*202del, NM_015106.2:c.*202del, NM_015106.2:c.*202dup, NM_015106.2:c.*201_*202dup, NM_015106.2:c.*200_*202dup, NM_015106.2:c.*199_*202dup, NM_015106.2:c.*196_*202dup, NM_015106.2:c.*195_*202dup, NM_015106.2:c.*194_*202dup, NM_015106.2:c.*193_*202dup, NM_015106.2:c.*192_*202dup, NM_015106.2:c.*190_*202dup, NM_015106.2:c.*181_*202dup, NM_015106.2:c.*178_*202dup, NM_001322253.2:c.*185_*198del, NM_001322253.2:c.*186_*198del, NM_001322253.2:c.*187_*198del, NM_001322253.2:c.*188_*198del, NM_001322253.2:c.*189_*198del, NM_001322253.2:c.*191_*198del, NM_001322253.2:c.*192_*198del, NM_001322253.2:c.*193_*198del, NM_001322253.2:c.*194_*198del, NM_001322253.2:c.*195_*198del, NM_001322253.2:c.*196_*198del, NM_001322253.2:c.*197_*198del, NM_001322253.2:c.*198del, NM_001322253.2:c.*198dup, NM_001322253.2:c.*197_*198dup, NM_001322253.2:c.*196_*198dup, NM_001322253.2:c.*195_*198dup, NM_001322253.2:c.*192_*198dup, NM_001322253.2:c.*191_*198dup, NM_001322253.2:c.*190_*198dup, NM_001322253.2:c.*189_*198dup, NM_001322253.2:c.*188_*198dup, NM_001322253.2:c.*186_*198dup, NM_001322253.2:c.*177_*198dup, NM_001322253.2:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001322253.1:c.*185_*198del, NM_001322253.1:c.*186_*198del, NM_001322253.1:c.*187_*198del, NM_001322253.1:c.*188_*198del, NM_001322253.1:c.*189_*198del, NM_001322253.1:c.*191_*198del, NM_001322253.1:c.*192_*198del, NM_001322253.1:c.*193_*198del, NM_001322253.1:c.*194_*198del, NM_001322253.1:c.*195_*198del, NM_001322253.1:c.*196_*198del, NM_001322253.1:c.*197_*198del, NM_001322253.1:c.*198del, NM_001322253.1:c.*198dup, NM_001322253.1:c.*197_*198dup, NM_001322253.1:c.*196_*198dup, NM_001322253.1:c.*195_*198dup, NM_001322253.1:c.*192_*198dup, NM_001322253.1:c.*191_*198dup, NM_001322253.1:c.*190_*198dup, NM_001322253.1:c.*189_*198dup, NM_001322253.1:c.*188_*198dup, NM_001322253.1:c.*186_*198dup, NM_001322253.1:c.*177_*198dup, NM_001322253.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001322256.2:c.*185_*198del, NM_001322256.2:c.*186_*198del, NM_001322256.2:c.*187_*198del, NM_001322256.2:c.*188_*198del, NM_001322256.2:c.*189_*198del, NM_001322256.2:c.*191_*198del, NM_001322256.2:c.*192_*198del, NM_001322256.2:c.*193_*198del, NM_001322256.2:c.*194_*198del, NM_001322256.2:c.*195_*198del, NM_001322256.2:c.*196_*198del, NM_001322256.2:c.*197_*198del, NM_001322256.2:c.*198del, NM_001322256.2:c.*198dup, NM_001322256.2:c.*197_*198dup, NM_001322256.2:c.*196_*198dup, NM_001322256.2:c.*195_*198dup, NM_001322256.2:c.*192_*198dup, NM_001322256.2:c.*191_*198dup, NM_001322256.2:c.*190_*198dup, NM_001322256.2:c.*189_*198dup, NM_001322256.2:c.*188_*198dup, NM_001322256.2:c.*186_*198dup, NM_001322256.2:c.*177_*198dup, NM_001322256.2:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001322256.1:c.*185_*198del, NM_001322256.1:c.*186_*198del, NM_001322256.1:c.*187_*198del, NM_001322256.1:c.*188_*198del, NM_001322256.1:c.*189_*198del, NM_001322256.1:c.*191_*198del, NM_001322256.1:c.*192_*198del, NM_001322256.1:c.*193_*198del, NM_001322256.1:c.*194_*198del, NM_001322256.1:c.*195_*198del, NM_001322256.1:c.*196_*198del, NM_001322256.1:c.*197_*198del, NM_001322256.1:c.*198del, NM_001322256.1:c.*198dup, NM_001322256.1:c.*197_*198dup, NM_001322256.1:c.*196_*198dup, NM_001322256.1:c.*195_*198dup, NM_001322256.1:c.*192_*198dup, NM_001322256.1:c.*191_*198dup, NM_001322256.1:c.*190_*198dup, NM_001322256.1:c.*189_*198dup, NM_001322256.1:c.*188_*198dup, NM_001322256.1:c.*186_*198dup, NM_001322256.1:c.*177_*198dup, NM_001322256.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001387866.1:c.*185_*198del, NM_001387866.1:c.*186_*198del, NM_001387866.1:c.*187_*198del, NM_001387866.1:c.*188_*198del, NM_001387866.1:c.*189_*198del, NM_001387866.1:c.*191_*198del, NM_001387866.1:c.*192_*198del, NM_001387866.1:c.*193_*198del, NM_001387866.1:c.*194_*198del, NM_001387866.1:c.*195_*198del, NM_001387866.1:c.*196_*198del, NM_001387866.1:c.*197_*198del, NM_001387866.1:c.*198del, NM_001387866.1:c.*198dup, NM_001387866.1:c.*197_*198dup, NM_001387866.1:c.*196_*198dup, NM_001387866.1:c.*195_*198dup, NM_001387866.1:c.*192_*198dup, NM_001387866.1:c.*191_*198dup, NM_001387866.1:c.*190_*198dup, NM_001387866.1:c.*189_*198dup, NM_001387866.1:c.*188_*198dup, NM_001387866.1:c.*186_*198dup, NM_001387866.1:c.*177_*198dup, NM_001387866.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001387867.1:c.*185_*198del, NM_001387867.1:c.*186_*198del, NM_001387867.1:c.*187_*198del, NM_001387867.1:c.*188_*198del, NM_001387867.1:c.*189_*198del, NM_001387867.1:c.*191_*198del, NM_001387867.1:c.*192_*198del, NM_001387867.1:c.*193_*198del, NM_001387867.1:c.*194_*198del, NM_001387867.1:c.*195_*198del, NM_001387867.1:c.*196_*198del, NM_001387867.1:c.*197_*198del, NM_001387867.1:c.*198del, NM_001387867.1:c.*198dup, NM_001387867.1:c.*197_*198dup, NM_001387867.1:c.*196_*198dup, NM_001387867.1:c.*195_*198dup, NM_001387867.1:c.*192_*198dup, NM_001387867.1:c.*191_*198dup, NM_001387867.1:c.*190_*198dup, NM_001387867.1:c.*189_*198dup, NM_001387867.1:c.*188_*198dup, NM_001387867.1:c.*186_*198dup, NM_001387867.1:c.*177_*198dup, NM_001387867.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001322257.1:c.*185_*198del, NM_001322257.1:c.*186_*198del, NM_001322257.1:c.*187_*198del, NM_001322257.1:c.*188_*198del, NM_001322257.1:c.*189_*198del, NM_001322257.1:c.*191_*198del, NM_001322257.1:c.*192_*198del, NM_001322257.1:c.*193_*198del, NM_001322257.1:c.*194_*198del, NM_001322257.1:c.*195_*198del, NM_001322257.1:c.*196_*198del, NM_001322257.1:c.*197_*198del, NM_001322257.1:c.*198del, NM_001322257.1:c.*198dup, NM_001322257.1:c.*197_*198dup, NM_001322257.1:c.*196_*198dup, NM_001322257.1:c.*195_*198dup, NM_001322257.1:c.*192_*198dup, NM_001322257.1:c.*191_*198dup, NM_001322257.1:c.*190_*198dup, NM_001322257.1:c.*189_*198dup, NM_001322257.1:c.*188_*198dup, NM_001322257.1:c.*186_*198dup, NM_001322257.1:c.*177_*198dup, NM_001322257.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001387869.1:c.*185_*198del, NM_001387869.1:c.*186_*198del, NM_001387869.1:c.*187_*198del, NM_001387869.1:c.*188_*198del, NM_001387869.1:c.*189_*198del, NM_001387869.1:c.*191_*198del, NM_001387869.1:c.*192_*198del, NM_001387869.1:c.*193_*198del, NM_001387869.1:c.*194_*198del, NM_001387869.1:c.*195_*198del, NM_001387869.1:c.*196_*198del, NM_001387869.1:c.*197_*198del, NM_001387869.1:c.*198del, NM_001387869.1:c.*198dup, NM_001387869.1:c.*197_*198dup, NM_001387869.1:c.*196_*198dup, NM_001387869.1:c.*195_*198dup, NM_001387869.1:c.*192_*198dup, NM_001387869.1:c.*191_*198dup, NM_001387869.1:c.*190_*198dup, NM_001387869.1:c.*189_*198dup, NM_001387869.1:c.*188_*198dup, NM_001387869.1:c.*186_*198dup, NM_001387869.1:c.*177_*198dup, NM_001387869.1:c.*198_*199insAAAAAAAAAAAAAAAAAAAAAAAAA

            6.

            rs1491510774 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              ->TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTT
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491506082 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->A [Show Flanks]
                Chromosome:
                3:51578307 (GRCh38)
                3:51612324 (GRCh37)
                Canonical SPDI:
                NC_000003.12:51578307:A:AA
                Gene:
                RAD54L2 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                AA=0./0 (ALFA)
                A=0.000004/1 (TOPMED)
                HGVS:

                8.

                rs1491500197 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  ->AG [Show Flanks]
                  Chromosome:
                  3:51581623 (GRCh38)
                  3:51615640 (GRCh37)
                  Canonical SPDI:
                  NC_000003.12:51581623:GAG:GAGAG
                  Gene:
                  RAD54L2 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  GAGAG=0.000071/1 (ALFA)
                  GA=0.000004/1 (TOPMED)
                  HGVS:

                  9.

                  rs1491461321 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    A>-,AA [Show Flanks]
                    Chromosome:
                    3:51620432 (GRCh38)
                    3:51654448 (GRCh37)
                    Canonical SPDI:
                    NC_000003.12:51620431:AA:A,NC_000003.12:51620431:AA:AAA
                    Gene:
                    RAD54L2 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAA=0./0 (ALFA)
                    -=0.000109/3 (TOMMO)
                    -=0.000289/39 (GnomAD)
                    HGVS:

                    10.

                    rs1491444698 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      3:51663594 (GRCh38)
                      3:51697610 (GRCh37)
                      Canonical SPDI:
                      NC_000003.12:51663593:CA:
                      Gene:
                      RAD54L2 (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      -=0.00084/10 (ALFA)
                      HGVS:

                      11.

                      rs1491414502 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        TG>- [Show Flanks]
                        Chromosome:
                        3:51581623 (GRCh38)
                        3:51615639 (GRCh37)
                        Canonical SPDI:
                        NC_000003.12:51581622:TG:
                        Gene:
                        RAD54L2 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        -=0.000224/1 (ALFA)
                        -=0.000007/1 (GnomAD)
                        -=0.000223/1 (Estonian)
                        HGVS:

                        12.

                        rs1491395008 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CA>- [Show Flanks]
                          Chromosome:
                          3:51597165 (GRCh38)
                          3:51631181 (GRCh37)
                          Canonical SPDI:
                          NC_000003.12:51597164:CA:
                          Gene:
                          RAD54L2 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          -=0./0 (ALFA)
                          HGVS:

                          13.

                          rs1491392319 has merged into rs71084151 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            TTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                            Chromosome:
                            3:51592065 (GRCh38)
                            3:51626081 (GRCh37)
                            Canonical SPDI:
                            NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51592054:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                            Gene:
                            RAD54L2 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTTTTTTTT=0./0 (ALFA)
                            TT=0.475/19 (GENOME_DK)
                            HGVS:
                            NC_000003.12:g.51592065_51592083del, NC_000003.12:g.51592066_51592083del, NC_000003.12:g.51592067_51592083del, NC_000003.12:g.51592068_51592083del, NC_000003.12:g.51592069_51592083del, NC_000003.12:g.51592070_51592083del, NC_000003.12:g.51592071_51592083del, NC_000003.12:g.51592072_51592083del, NC_000003.12:g.51592073_51592083del, NC_000003.12:g.51592074_51592083del, NC_000003.12:g.51592075_51592083del, NC_000003.12:g.51592076_51592083del, NC_000003.12:g.51592077_51592083del, NC_000003.12:g.51592080_51592083del, NC_000003.12:g.51592081_51592083del, NC_000003.12:g.51592082_51592083del, NC_000003.12:g.51592083del, NC_000003.12:g.51592083dup, NC_000003.12:g.51592082_51592083dup, NC_000003.12:g.51592081_51592083dup, NC_000003.12:g.51592080_51592083dup, NC_000003.12:g.51592079_51592083dup, NC_000003.12:g.51592078_51592083dup, NC_000003.12:g.51592077_51592083dup, NC_000003.12:g.51592076_51592083dup, NC_000003.12:g.51592075_51592083dup, NC_000003.12:g.51592074_51592083dup, NC_000003.12:g.51592073_51592083dup, NC_000003.12:g.51592072_51592083dup, NC_000003.12:g.51592071_51592083dup, NC_000003.12:g.51592068_51592083dup, NC_000003.12:g.51592066_51592083dup, NC_000003.12:g.51592061_51592083dup, NC_000003.12:g.51592060_51592083dup, NC_000003.12:g.51592058_51592083dup, NC_000003.12:g.51592056_51592083dup, NC_000003.12:g.51592083_51592084insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51592083_51592084insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51626081_51626099del, NC_000003.11:g.51626082_51626099del, NC_000003.11:g.51626083_51626099del, NC_000003.11:g.51626084_51626099del, NC_000003.11:g.51626085_51626099del, NC_000003.11:g.51626086_51626099del, NC_000003.11:g.51626087_51626099del, NC_000003.11:g.51626088_51626099del, NC_000003.11:g.51626089_51626099del, NC_000003.11:g.51626090_51626099del, NC_000003.11:g.51626091_51626099del, NC_000003.11:g.51626092_51626099del, NC_000003.11:g.51626093_51626099del, NC_000003.11:g.51626096_51626099del, NC_000003.11:g.51626097_51626099del, NC_000003.11:g.51626098_51626099del, NC_000003.11:g.51626099del, NC_000003.11:g.51626099dup, NC_000003.11:g.51626098_51626099dup, NC_000003.11:g.51626097_51626099dup, NC_000003.11:g.51626096_51626099dup, NC_000003.11:g.51626095_51626099dup, NC_000003.11:g.51626094_51626099dup, NC_000003.11:g.51626093_51626099dup, NC_000003.11:g.51626092_51626099dup, NC_000003.11:g.51626091_51626099dup, NC_000003.11:g.51626090_51626099dup, NC_000003.11:g.51626089_51626099dup, NC_000003.11:g.51626088_51626099dup, NC_000003.11:g.51626087_51626099dup, NC_000003.11:g.51626084_51626099dup, NC_000003.11:g.51626082_51626099dup, NC_000003.11:g.51626077_51626099dup, NC_000003.11:g.51626076_51626099dup, NC_000003.11:g.51626074_51626099dup, NC_000003.11:g.51626072_51626099dup, NC_000003.11:g.51626099_51626100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51626099_51626100insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                            14.

                            rs1491351999 [Homo sapiens]
                              Variant type:
                              DEL
                              Alleles:
                              CA>- [Show Flanks]
                              Chromosome:
                              3:51541040 (GRCh38)
                              3:51575056 (GRCh37)
                              Canonical SPDI:
                              NC_000003.12:51541039:CA:
                              Gene:
                              RAD54L2 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              -=0.00042/5 (ALFA)
                              -=0.00103/29 (TOMMO)
                              HGVS:

                              15.

                              rs1491327294 [Homo sapiens]
                                Variant type:
                                SNV:
                                Alleles:
                                ->TTTTT
                                Chromosome:
                                no mapping
                                Canonical SPDI:

                                16.

                                rs1491326444 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  GA>- [Show Flanks]
                                  Chromosome:
                                  3:51557855 (GRCh38)
                                  3:51591871 (GRCh37)
                                  Canonical SPDI:
                                  NC_000003.12:51557853:AGA:A
                                  Gene:
                                  RAD54L2 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0./0 (ALFA)
                                  -=0.000004/1 (TOPMED)
                                  -=0.000014/2 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1491310480 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    AG>- [Show Flanks]
                                    Chromosome:
                                    3:51668086 (GRCh38)
                                    3:51702102 (GRCh37)
                                    Canonical SPDI:
                                    NC_000003.12:51668084:GAG:G
                                    Gene:
                                    RAD54L2 (Varview)
                                    Functional Consequence:
                                    3_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0.000422/5 (ALFA)
                                    -=0.001056/145 (GnomAD)
                                    -=0.001168/20 (TOMMO)
                                    -=0.003236/12 (TWINSUK)
                                    -=0.003373/13 (ALSPAC)
                                    -=0.003821/7 (Korea1K)
                                    -=0.02/12 (NorthernSweden)
                                    HGVS:

                                    18.

                                    rs1491280269 [Homo sapiens]
                                      Variant type:
                                      SNV:
                                      Alleles:
                                      TA>-
                                      Chromosome:
                                      no mapping
                                      Canonical SPDI:

                                      19.

                                      rs1491266867 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        ->CTTTTTTT [Show Flanks]
                                        Chromosome:
                                        3:51560363 (GRCh38)
                                        3:51594380 (GRCh37)
                                        Canonical SPDI:
                                        NC_000003.12:51560363:TTTTTTT:TTTTTTTCTTTTTTT
                                        Gene:
                                        RAD54L2 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        TTTTTTTCTTTTTTT=0./0 (ALFA)
                                        HGVS:

                                        20.

                                        rs1491257099 has merged into rs61245532 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TT>-,T,TTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                          Chromosome:
                                          3:51582775 (GRCh38)
                                          3:51616791 (GRCh37)
                                          Canonical SPDI:
                                          NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                          Gene:
                                          RAD54L2 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TTTTTTTTT=0./0 (ALFA)
                                          -=0.000008/2 (TOPMED)
                                          HGVS:
                                          NC_000003.12:g.51582775_51582776del, NC_000003.12:g.51582776del, NC_000003.12:g.51582776dup, NC_000003.12:g.51582772_51582776dup, NC_000003.12:g.51582771_51582776dup, NC_000003.12:g.51582770_51582776dup, NC_000003.12:g.51582769_51582776dup, NC_000003.12:g.51582768_51582776dup, NC_000003.12:g.51582767_51582776dup, NC_000003.12:g.51582776_51582777insTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616791_51616792del, NC_000003.11:g.51616792del, NC_000003.11:g.51616792dup, NC_000003.11:g.51616788_51616792dup, NC_000003.11:g.51616787_51616792dup, NC_000003.11:g.51616786_51616792dup, NC_000003.11:g.51616785_51616792dup, NC_000003.11:g.51616784_51616792dup, NC_000003.11:g.51616783_51616792dup, NC_000003.11:g.51616792_51616793insTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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