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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917212copy number variation1nstd229human GRCh38 chr11: 45,767,701-45,770,100 , GRCh37.p13 chr11: 45,789,252-45,791,651 LINC02716
    nsv6907910copy number variation1nstd229human GRCh38 chr11: 45,659,580-45,829,818 , GRCh37.p13 chr11: 45,681,130-45,851,369 LINC02716, LINC02690, 4 more genes
    nsv6472910copy number variation1nstd223human GRCh38 chr11: 45,767,690-45,770,069 , GRCh37.p13 chr11: 45,789,241-45,791,620 LINC02716
    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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6291214copy number variation1nstd102humanUncertain significance GRCh37 chr11: 45,675,636-45,850,138 , GRCh38.p12 chr11: 45,654,086-45,828,587 LINC02690, SLC35C1, 4 more genes
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 more genes
    nsv6143810copy number variation1nstd206human GRCh38 chr11: 45,758,434-45,785,223 , GRCh37.p13 chr11: 45,779,985-45,806,774 LINC02716
    nsv6028160copy number variation1nstd212human GRCh38 chr11: 45,753,584-45,774,973 , GRCh37.p13 chr11: 45,775,135-45,796,524 LINC02716
    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
    nsv4970938copy number variation1nstd200human GRCh38 chr11: 45,768,264-45,770,617 , GRCh37.p13 chr11: 45,789,815-45,792,168 LINC02716
    nsv4970937copy number variation1nstd200human GRCh38 chr11: 45,767,690-45,770,069 , GRCh37.p13 chr11: 45,789,241-45,791,620 LINC02716
    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
    nsv4729649copy number variation1nstd102humanUncertain significance GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245 LOC105376654, PHF21A, 31 more genes
    nsv4714830copy number variation1nstd195human GRCh37 chr11: 45,760,601-46,177,151 , GRCh38.p12 chr11: 45,739,050-46,155,600 SLC35C1, LINC02716, 9 more genes
    nsv4563167mobile element insertion1nstd166human GRCh37.p13 chr11: 45,792,411-45,792,411 , GRCh38.p12 chr11: 45,770,860-45,770,860 LINC02716
    nsv4211354copy number variation1nstd166human GRCh37.p13 chr11: 45,789,241-45,791,620 , GRCh38.p12 chr11: 45,767,690-45,770,069 LINC02716
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3922177copy number variation1nstd102humanPathogenic GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947 MIR3160-2, LOC105376631, 122 more genes
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