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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6916237copy number variation1nstd229human GRCh38 chr11: 4,369,424-4,697,710 , GRCh37.p13 chr11: 4,390,654-4,718,940 TRIM68, OR51E2, 17 more genes
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6914951copy number variation1nstd229human GRCh38 chr11: 4,515,180-4,719,642 , GRCh37.p13 chr11: 4,536,410-4,740,872 OR51A9P, OR52M1, 12 more genes
    nsv6909179copy number variation1nstd229human GRCh38 chr11: 4,697,745-4,697,934 , GRCh37.p13 chr11: 4,718,975-4,719,164 OR51E2
    nsv6907513copy number variation1nstd229human GRCh38 chr11: 4,674,418-4,722,016 , GRCh37.p13 chr11: 4,695,648-4,743,246 OR51C1P, KRT8P49, 3 more genes
    nsv6903025copy number variation1nstd229human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51V1, OR51L1, 39 more genes
    nsv6902995copy number variation1nstd229human GRCh38 chr11: 4,619,101-5,268,938 , GRCh37.p13 chr11: 4,640,331-5,290,168 OR51A9P, OR51F1, 50 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6450577copy number variation1nstd223human GRCh38 chr11: 4,619,075-5,268,953 , GRCh37.p13 chr11: 4,640,305-5,290,183 OR52J1P, OR51F2, 50 more genes
    nsv6447188copy number variation1nstd223human GRCh38 chr11: 4,683,958-4,688,381 , GRCh37.p13 chr11: 4,705,188-4,709,611 OR51E2
    nsv6439692copy number variation1nstd223human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51S1, OR51F1, 39 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    nsv6131826copy number variation1nstd213human GRCh37 chr11: 4,710,758-4,802,234 , GRCh38.p12 chr11: 4,689,528-4,781,004 OR51E2, OR51F1, 6 more genes
    nsv5337262translocation1nstd200human GRCh37 chr11: 4,717,875-4,717,875 , GRCh37 chr11: 4,544,640-4,544,640 , GRCh38.p12 chr11: 4,696,645-4,696,645 , GRCh38.p12 chr11: 4,523,410-4,523,410 OR51E2
    nsv5322829translocation1nstd204human GRCh38.p13 chr11: 4,523,410-4,523,410 , GRCh38.p13 chr11: 4,696,645-4,696,645 , GRCh37.p13 chr11: 4,544,640-4,544,640 , GRCh37.p13 chr11: 4,717,875-4,717,875 OR51E2
    nsv5259243copy number variation1nstd204human GRCh37.p13 chr11: 4,642,231-4,717,830 , GRCh38.p13 chr11: 4,621,001-4,696,600 OR51E2, OR51E1, 4 more genes
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