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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093698copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,411,829-6,662,844 , GRCh38.p12 chr11: 6,390,599-6,641,613 SMPD1, HPX, 11 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6915941copy number variation1nstd229human GRCh38 chr11: 6,431,542-6,432,138 , GRCh37.p13 chr11: 6,452,772-6,453,368 HPX
    nsv6911748copy number variation1nstd229human GRCh38 chr11: 6,314,301-6,441,800 , GRCh37.p13 chr11: 6,335,531-6,463,030 HPX, CAVIN3, 3 more genes
    nsv6905999copy number variation1nstd229human GRCh38 chr11: 6,428,413-6,430,695 , GRCh37.p13 chr11: 6,449,643-6,451,925 HPX
    nsv6900827copy number variation1nstd229human GRCh38 chr11: 6,191,411-6,542,996 , GRCh37.p13 chr11: 6,212,641-6,564,226 ARFIP2, RRP8, 14 more genes
    nsv6898535copy number variation1nstd229human GRCh38 chr11: 6,437,340-6,446,026 , GRCh37.p13 chr11: 6,458,570-6,467,256 HPX
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6448117copy number variation1nstd223human GRCh38 chr11: 6,421,538-6,464,910 , GRCh37.p13 chr11: 6,442,768-6,486,140 TRIM3, HPX
    nsv6446051copy number variation1nstd223human GRCh38 chr11: 6,428,577-6,437,175 , GRCh37.p13 chr11: 6,449,807-6,458,405 HPX
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6277728insertion1nstd214human GRCh38 chr11: 6,436,002-6,436,002 , GRCh37.p13 chr11: 6,457,232-6,457,232 HPX
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 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
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4496011mobile element insertion1nstd166human GRCh37.p13 chr11: 6,459,264-6,459,264 , GRCh38.p12 chr11: 6,438,034-6,438,034 HPX
    nsv4456235copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621 OR52X1P, LOC112268071, 40 more genes
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