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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5501765copy number variation1nstd206human GRCh38 chr11: 109,427,774-109,427,824 , GRCh37.p13 chr11: 109,298,500-109,298,550 C11orf87
    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
    nsv5300853copy number variation1nstd204human GRCh38.p13 chr11: 109,431,428-109,431,579 , GRCh37.p13 chr11: 109,302,154-109,302,305 C11orf87
    nsv4980600copy number variation1nstd200human GRCh38 chr11: 109,432,519-109,432,614 , GRCh37.p13 chr11: 109,303,245-109,303,340 C11orf87
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675477copy number variation1nstd102humanUncertain significance GRCh37 chr11: 109,123,216-109,349,434 , GRCh38.p12 chr11: 109,252,489-109,478,708 C11orf87
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4558081mobile element insertion1nstd166human GRCh37.p13 chr11: 109,302,319-109,302,319 , GRCh38.p12 chr11: 109,431,593-109,431,593 C11orf87
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4210769copy number variation1nstd166human GRCh37.p13 chr11: 109,291,494-109,292,400 , GRCh38.p12 chr11: 109,420,768-109,421,674 C11orf87
    nsv4210389copy number variation1nstd166human GRCh37.p13 chr11: 109,303,245-109,303,340 , GRCh38.p12 chr11: 109,432,519-109,432,614 C11orf87
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3913577copy number variation1nstd102humanPathogenic NCBI36 chr11: 105,972,805-113,384,939 , GRCh37.p13 chr11: 106,467,595-113,879,729 , GRCh38.p12 chr11: 106,596,868-114,009,007 LAYN, DDX10, 133 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 LOC101060084, PGAM1P9, 230 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 more genes
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