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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
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6910053copy number variation1nstd229human GRCh38 chr11: 62,363,901-63,050,100 , GRCh37.p13 chr11: 62,131,373-62,817,572 MIR6747, TMEM179B, 54 more genes
    nsv6908114copy number variation1nstd229human GRCh38 chr11: 62,593,901-63,028,400 , GRCh37.p13 chr11: 62,361,373-62,795,872 GANAB, SLC22A6, 44 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
    nsv6904565copy number variation1nstd229human GRCh38 chr11: 62,240,001-63,046,600 , GRCh37.p13 chr11: 62,007,473-62,814,072 RCC2P6, SNORD26, 58 more genes
    nsv6903779copy number variation1nstd229human GRCh38 chr11: 62,796,669-62,913,409 , GRCh37.p13 chr11: 62,564,141-62,680,881 SNORD30, STX5-DT, 16 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
    nsv6900187copy number variation1nstd229human GRCh38 chr11: 62,838,248-62,866,261 , GRCh37.p13 chr11: 62,605,720-62,633,733 WDR74, SNORD30, 10 more genes
    nsv6474621copy number variation1nstd223human GRCh38 chr11: 62,852,425-62,852,807 , GRCh37.p13 chr11: 62,619,897-62,620,279 SNORD29, SNORD31, 4 more genes
    nsv6464851copy number variation1nstd223human GRCh38 chr11: 62,831,466-62,852,682 , GRCh37.p13 chr11: 62,598,938-62,620,154 STX5, WDR74, 8 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
    nsv6131999copy number variation1nstd213human GRCh37 chr11: 62,579,390-62,707,802 , GRCh38.p12 chr11: 62,811,918-62,940,330 SNORD27, SNORD22, 16 more genes
    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
    nsv5373661translocation1nstd200human GRCh37.p13 chr11: 62,598,938-62,598,938 , GRCh37.p13 chr11: 62,620,154-62,620,154 , GRCh38 chr11: 62,831,466-62,831,466 , GRCh38 chr11: 62,852,682-62,852,682 STX5, SNORD29, 7 more genes
    nsv5264892copy number variation1nstd204human GRCh38.p13 chr11: 62,843,236-62,855,465 , GRCh37.p13 chr11: 62,610,708-62,622,937 SLC3A2, SNORD26, 8 more genes
    nsv4838332copy number variation1nstd200human GRCh37 chr11: 62,618,989-62,619,656 , GRCh38.p12 chr11: 62,851,517-62,852,184 SNORD30, SNORD29, 3 more genes
    nsv4830338copy number variation1nstd200human GRCh37 chr11: 62,598,938-62,620,154 , GRCh38.p12 chr11: 62,831,466-62,852,682 SNORD30, STX5-DT, 8 more genes
    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
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