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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112723copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,566,891-178,585,880 , GRCh38.p12 chr5: 179,139,890-179,158,879 ADAMTS2
    nsv5965088insertion1nstd209human GRCh38 chr5: 179,140,799-179,140,799 , GRCh37.p13 chr5: 178,567,800-178,567,800 ADAMTS2
    nsv5960817insertion1nstd209human GRCh38 chr5: 179,264,873-179,264,873 , GRCh37.p13 chr5: 178,691,874-178,691,874 ADAMTS2
    nsv5951172insertion1nstd209human GRCh38 chr5: 179,217,855-179,217,855 , GRCh37.p13 chr5: 178,644,856-178,644,856 ADAMTS2
    nsv5907065copy number variation1nstd209human GRCh38 chr5: 179,212,237-179,212,287 , GRCh37.p13 chr5: 178,639,238-178,639,288 ADAMTS2
    nsv5905452copy number variation1nstd209human GRCh38 chr5: 179,322,360-179,322,487 , GRCh37.p13 chr5: 178,749,361-178,749,488 ADAMTS2
    nsv5904407copy number variation1nstd209human GRCh38 chr5: 179,277,349-179,277,846 , GRCh37.p13 chr5: 178,704,350-178,704,847 ADAMTS2
    nsv5903599copy number variation1nstd209human GRCh38 chr5: 179,129,180-179,129,336 , GRCh37.p13 chr5: 178,556,181-178,556,337 ADAMTS2
    nsv5893188copy number variation1nstd209human GRCh38 chr5: 179,134,746-179,135,037 , GRCh37.p13 chr5: 178,561,747-178,562,038 ADAMTS2
    nsv5891066copy number variation1nstd209human GRCh38 chr5: 179,316,059-179,316,894 , GRCh37.p13 chr5: 178,743,060-178,743,895 ADAMTS2
    nsv5888744copy number variation1nstd209human GRCh38 chr5: 179,110,070-179,110,194 , GRCh37.p13 chr5: 178,537,071-178,537,195 ADAMTS2
    nsv5887663copy number variation1nstd209human GRCh38 chr5: 179,214,140-179,214,289 , GRCh37.p13 chr5: 178,641,141-178,641,290 ADAMTS2
    nsv5842235copy number variation1nstd209human GRCh38 chr5: 179,322,549-179,348,469 , GRCh37.p13 chr5: 178,749,550-178,775,470 ADAMTS2, LOC105377759
    nsv5842234copy number variation1nstd209human GRCh38 chr5: 179,309,761-179,311,860 , GRCh37.p13 chr5: 178,736,762-178,738,861 ADAMTS2
    nsv5842233copy number variation1nstd209human GRCh38 chr5: 179,299,092-179,318,548 , GRCh37.p13 chr5: 178,726,093-178,745,549 ADAMTS2
    nsv5841933copy number variation1nstd209human GRCh38 chr5: 179,321,124-179,327,289 , GRCh37.p13 chr5: 178,748,125-178,754,290 ADAMTS2
    nsv5841932copy number variation1nstd209human GRCh38 chr5: 179,278,252-179,280,651 , GRCh37.p13 chr5: 178,705,253-178,707,652 ADAMTS2
    nsv5673760copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 178,554,950-178,564,955 , GRCh38.p12 chr5: 179,127,949-179,137,954 ADAMTS2
    nsv5673584copy number variation1nstd102humanPathogenic GRCh37 chr5: 178,699,902-178,772,339 , GRCh38.p12 chr5|NW_016107298.1: 37,608-110,045 , GRCh38.p12 chr5: 179,272,901-179,345,338 ADAMTS2, LOC105377759
    nsv5642351insertion1nstd207human GRCh38 chr5: 179,277,946-179,277,946 , GRCh37.p13 chr5: 178,704,947-178,704,947 ADAMTS2
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