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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7058567inversion1nstd229human GRCh38 chr11: 64,369,149-64,413,060 , GRCh37.p13 chr11: 64,136,621-64,180,532 MIR1237, RPS6KA4, 2 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6132371copy number variation1nstd213human GRCh37 chr11: 63,120,000-64,210,001 , GRCh38.p12 chr11: 63,352,528-64,442,529 VEGFB, FLRT1, 51 more genes
    nsv6132111copy number variation1nstd213human GRCh37 chr11: 63,900,000-64,180,001 , GRCh38.p12 chr11: 64,132,528-64,412,529 ESRRA, DNAJC4, 26 more genes
    nsv5653393insertion1nstd207human GRCh38 chr11: 64,366,904-64,366,904 , GRCh37.p13 chr11: 64,134,376-64,134,376 MIR1237, RPS6KA4
    nsv5647095insertion1nstd207human GRCh38 chr11: 64,368,090-64,368,090 , GRCh37.p13 chr11: 64,135,562-64,135,562 RPS6KA4, MIR1237
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355282translocation1nstd200human GRCh38 chr11: 64,368,797-64,368,797 , GRCh38 chr11: 64,369,442-64,369,442 , GRCh37.p13 chr11: 64,136,269-64,136,269 , GRCh37.p13 chr11: 64,136,914-64,136,914 MIR1237, RPS6KA4
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5132670mobile element insertion1nstd203human GRCh38 chr11: 64,367,939-64,367,954 , GRCh37.p13 chr11: 64,135,411-64,135,426 MIR1237, RPS6KA4
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4666118copy number variation2nstd186human GRCh37 chr11: 64,136,117-64,136,176 , GRCh38.p12 chr11: 64,368,645-64,368,704 RPS6KA4, MIR1237
    nsv4611133copy number variation2nstd183human GRCh37 chr11: 64,136,117-64,136,176 , GRCh38.p12 chr11: 64,368,645-64,368,704 MIR1237, RPS6KA4
    nsv4609656copy number variation1nstd183human GRCh37 chr11: 64,136,117-64,137,247 , GRCh38.p12 chr11: 64,368,645-64,369,775 RPS6KA4, MIR1237
    nsv4600105copy number variation1nstd183human GRCh37 chr11: 64,135,905-64,137,247 , GRCh38.p12 chr11: 64,368,433-64,369,775 MIR1237, RPS6KA4
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
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