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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6993186copy number variation1nstd229human GRCh38 chr17: 46,736,426-46,737,038 , GRCh37.p13 chr17: 44,813,792-44,814,404 LRRC37A2, NSF
    nsv6986819copy number variation1nstd229human GRCh38 chr17: 46,753,286-46,798,729 , GRCh37.p13 chr17: 44,830,652-44,876,095 NSF, WNT3, 1 more genes
    nsv6983590copy number variation1nstd229human GRCh38 chr17: 46,711,339-46,917,487 , GRCh37.p13 chr17: 44,788,705-44,994,853 NSF, WNT3, 7 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6624285copy number variation1nstd224human GRCh37 chr17: 44,248,394-44,800,110 , GRCh38.p12 chr17: 46,171,028-46,722,744 , GRCh38.p12 chr17|NT_187663.1: 873,133-1,242,173 NSF, KANSL1-AS1, 14 more genes
    nsv6624279copy number variation3nstd224human GRCh37 chr17: 44,169,808-44,800,110 , GRCh38.p12 chr17: 46,092,442-46,722,744 , GRCh38.p12 chr17|NT_187663.1: 794,550-1,242,173 LRRC37A2, RPS7P11, 15 more genes
    nsv6586640inversion1nstd223human GRCh38 chr17: 46,708,022-46,708,512 , GRCh37.p13 chr17: 44,785,388-44,785,878 NSF, LRRC37A2
    nsv6577399inversion1nstd223human GRCh38 chr17: 46,707,771-46,708,594 , GRCh37.p13 chr17: 44,785,137-44,785,960 LRRC37A2, NSF
    nsv6575722inversion1nstd223human GRCh38 chr17: 46,739,091-46,739,953 , GRCh37.p13 chr17: 44,816,457-44,817,319 NSF, LRRC37A2
    nsv6535295copy number variation1nstd223human GRCh38 chr17: 46,733,801-46,734,700 , GRCh37.p13 chr17: 44,811,167-44,812,066 NSF, LRRC37A2
    nsv6533512copy number variation1nstd223human GRCh38 chr17: 46,731,347-46,731,936 , GRCh37.p13 chr17: 44,808,713-44,809,302 LRRC37A2, NSF
    nsv6516978copy number variation1nstd223human GRCh38 chr17: 46,719,790-46,721,896 , GRCh37.p13 chr17: 44,797,156-44,799,262 RPS7P11, LRRC37A2, 1 more genes
    nsv6497344copy number variation1nstd223human GRCh38 chr17: 46,098,250-47,084,546 , GRCh37.p13 chr17: 44,175,616-45,161,912 ARL17A, MIR5089, 27 more genes
    nsv6307356copy number variation1nstd186human GRCh37 chr17: 44,775,346-44,781,346 , GRCh38.p12 chr17: 46,697,980-46,703,980 , GRCh38.p12 chr17|NT_187663.1: 1,217,407-1,223,405 , GRCh38.p12 chr17|NT_167251.2: 1,683,869-1,689,869 NSF, LRRC37A2
    nsv6307173copy number variation1nstd186human GRCh37 chr17: 44,369,346-44,782,506 , GRCh38.p12 chr17|NT_187663.1: 1,009,112-1,224,565 , GRCh38.p12 chr17: 46,291,980-46,705,140 , FAM215B, 8 more genes
    nsv6307094copy number variation1nstd186human GRCh37 chr17: 44,763,346-44,779,346 , GRCh38.p12 chr17: 46,685,980-46,701,980 , GRCh38.p12 chr17|NT_187663.1: 1,205,403-1,221,405 , GRCh38.p12 chr17|NT_167251.2: 1,671,870-1,687,869 LRRC37A2, NSF
    nsv6306996copy number variation1nstd186human GRCh37 chr17: 44,708,766-44,715,346 , GRCh38.p12 chr17: 46,631,400-46,637,980 , GRCh38.p12 chr17|NT_187663.1: 1,151,077-1,157,663 LRRC37A2, NSF
    nsv6306896copy number variation1nstd186human GRCh37 chr17: 44,720,166-44,739,346 , GRCh38.p12 chr17: 46,642,800-46,661,980 , GRCh38.p12 chr17|NT_187663.1: 1,162,483-1,181,544 LRRC37A2, NSF
    nsv6306226copy number variation1nstd186human GRCh37 chr17: 44,689,346-44,695,346 , GRCh38.p12 chr17: 46,611,980-46,617,980 , GRCh38.p12 chr17|NT_187663.1: 1,131,655-1,137,657 NSF, LRRC37A2
    nsv6146094copy number variation1nstd206human GRCh38 chr17: 46,685,980-46,701,980 , GRCh37.p13 chr17: 44,763,346-44,779,346 LRRC37A2, NSF
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