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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914180copy number variation1nstd209human GRCh38 chr10: 9,716,056-9,744,824 , GRCh37.p13 chr10: 9,758,019-9,786,787 LINC02663, HSP90AB7P
    nsv5866160copy number variation1nstd209human GRCh38 chr10: 9,716,023-9,729,463 , GRCh37.p13 chr10: 9,757,986-9,771,426 LINC02663, HSP90AB7P
    nsv5537228insertion1nstd206human GRCh38 chr10: 9,720,112-9,720,136 , GRCh37.p13 chr10: 9,762,075-9,762,099 LINC02663, HSP90AB7P
    nsv5487438copy number variation1nstd206human GRCh38 chr10: 9,701,322-9,832,818 , GRCh37.p13 chr10: 9,743,285-9,874,781 HSP90AB7P, LINC02663
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5301016copy number variation1nstd204human GRCh37.p13 chr10: 9,691,998-9,824,783 , GRCh38.p13 chr10: 9,650,035-9,782,820 HSP90AB7P, LINC02663
    nsv5253993copy number variation1nstd204human GRCh38.p13 chr10: 9,650,101-9,782,800 , GRCh37.p13 chr10: 9,692,064-9,824,763 LINC02663, HSP90AB7P
    nsv5253959copy number variation1nstd204human GRCh38.p13 chr10: 9,703,810-9,733,365 , GRCh37.p13 chr10: 9,745,773-9,775,328 LINC02663, HSP90AB7P
    nsv4969579copy number variation1nstd200human GRCh38 chr10: 9,716,056-9,744,825 , GRCh37.p13 chr10: 9,758,019-9,786,788 LINC02663, HSP90AB7P
    nsv4969576copy number variation1nstd200human GRCh38 chr10: 9,670,405-9,856,910 , GRCh37.p13 chr10: 9,712,368-9,898,873 HSP90AB7P, LINC02663
    nsv4842240copy number variation1nstd200human GRCh37 chr10: 9,758,019-9,786,788 , GRCh38.p12 chr10: 9,716,056-9,744,825 HSP90AB7P, LINC02663
    nsv4680171copy number variation1nstd189human GRCh38.p12 chr10: 9,460,711-9,858,942 , GRCh37.p13 chr10: 9,502,674-9,900,905 HSP90AB7P, LINC02663
    nsv4679560copy number variation1nstd189human GRCh37.p13 chr10: 9,302,856-10,277,312 , GRCh38.p12 chr10: 9,260,893-10,235,349 , HSP90AB7P, 6 more genes
    nsv4599381copy number variation1nstd183human GRCh37 chr10: 9,715,294-9,896,924 , GRCh38.p12 chr10: 9,673,331-9,854,961 LINC02663, HSP90AB7P
    nsv4455884copy number variation1nstd102humanPathogenic GRCh37 chr10: 8,011,156-9,996,086 , GRCh38.p12 chr10: 7,969,193-9,954,123 LOC105376396, KRT8P37, 22 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4377886copy number variation1nstd173human GRCh37 chr10: 9,510,657-9,901,226 , GRCh38.p12 chr10: 9,468,694-9,859,263 LINC02663, HSP90AB7P
    nsv4373910copy number variation1nstd173human GRCh37 chr10: 9,513,578-9,901,226 , GRCh38.p12 chr10: 9,471,615-9,859,263 HSP90AB7P, LINC02663
    nsv4368256copy number variation1nstd173human GRCh37 chr10: 9,510,657-9,904,799 , GRCh38.p12 chr10: 9,468,694-9,862,836 LINC02663, HSP90AB7P
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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