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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv6910311copy number variation1nstd229human GRCh38 chr11: 71,721,399-71,910,691 , GRCh37.p13 chr11: 71,432,445-71,621,737 RNA5SP342, FAM86C1P, 9 more genes
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6472495copy number variation1nstd223human GRCh38 chr11: 71,600,178-71,900,170 , GRCh37.p13 chr11: 71,311,224-71,611,216 DEFB130C, ENPP7P8, 13 more genes
    nsv6465046copy number variation1nstd223human GRCh38 chr11: 71,806,201-71,841,400 , GRCh37.p13 chr11: 71,517,247-71,552,446 ZNF705EP, DEFB108B, 1 more genes
    nsv6462604copy number variation1nstd223human GRCh38 chr11: 71,587,217-71,887,226 , GRCh37.p13 chr11: 71,298,263-71,598,272 RPS3AP41, XNDC1N, 13 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
    nsv5921996copy number variation1nstd209human GRCh38 chr11: 71,812,132-71,812,216 , GRCh37.p13 chr11: 71,523,178-71,523,262 ALG1L9P, ZNF705EP
    nsv5857551copy number variation1nstd209human GRCh38 chr11: 71,805,790-71,827,343 , GRCh37.p13 chr11: 71,516,836-71,538,389 ZNF705EP, ALG1L9P
    nsv5725222mobile element insertion1nstd211human GRCh38 chr11: 71,812,049-71,812,049 , GRCh37.p13 chr11: 71,523,095-71,523,095 ZNF705EP, ALG1L9P
    nsv5586670copy number variation1nstd207human GRCh38 chr11: 71,600,639-71,900,634 , GRCh37.p13 chr11: 71,311,685-71,611,680 , OR7E128P, 14 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
    nsv5355351translocation1nstd200human GRCh38 chr11: 71,812,132-71,812,132 , GRCh38 chr11: 71,812,217-71,812,217 , GRCh37.p13 chr11: 71,523,263-71,523,263 , GRCh37.p13 chr11: 71,523,178-71,523,178 ALG1L9P, ZNF705EP
    nsv5197485mobile element insertion1nstd203human GRCh38 chr11: 71,812,040-71,812,049 , GRCh37.p13 chr11: 71,523,086-71,523,095 ALG1L9P, ZNF705EP
    nsv5194296mobile element insertion1nstd203human GRCh38 chr11: 71,812,035-71,812,049 , GRCh37.p13 chr11: 71,523,081-71,523,095 ZNF705EP, ALG1L9P
    nsv4980094copy number variation1nstd200human GRCh38 chr11: 71,686,395-71,876,337 , GRCh37.p13 chr11: 71,397,441-71,587,383 , ALG1L9P, 8 more genes
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4614835copy number variation2nstd183human GRCh37 chr11: 71,513,490-71,555,712 , GRCh38.p12 chr11: 71,802,444-71,844,666 DEFB108B, ALG1L9P, 2 more genes
    nsv4612418copy number variation1nstd183human GRCh37 chr11: 71,498,860-71,553,549 , GRCh38.p12 chr11: 71,787,814-71,842,503 DEFB108B, FAM86C1P, 2 more genes
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