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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093727copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,111,299-73,122,365 , GRCh38.p12 chr10: 71,351,542-71,362,608 SLC29A3
    nsv7093645copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,121,691-73,122,365 , GRCh38.p12 chr10: 71,361,934-71,362,608 SLC29A3
    nsv7093644copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,115,818-73,116,020 , GRCh38.p12 chr10: 71,356,061-71,356,263 SLC29A3
    nsv7075866inversion1nstd229human GRCh38 chr10: 71,314,808-71,434,396 , GRCh37.p13 chr10: 73,074,565-73,194,153 CDH23, LOC105378353, 1 more genes
    nsv7058306inversion1nstd229human GRCh38 chr10: 71,209,770-71,317,966 , GRCh37.p13 chr10: 72,969,527-73,077,723 SLC29A3, LOC112268061, 2 more genes
    nsv6897657copy number variation1nstd229human GRCh38 chr10: 71,288,245-71,625,893 , GRCh37.p13 chr10: 73,048,002-73,385,650 LOC105378353, UNC5B, 5 more genes
    nsv6896859copy number variation1nstd229human GRCh38 chr10: 71,362,723-71,367,162 , GRCh37.p13 chr10: 73,122,480-73,126,919 SLC29A3
    nsv6896040copy number variation1nstd229human GRCh38 chr10: 71,337,458-71,341,296 , GRCh37.p13 chr10: 73,097,215-73,101,053 LOC105378353, SLC29A3
    nsv6893833copy number variation1nstd229human GRCh38 chr10: 71,331,501-71,365,800 , GRCh37.p13 chr10: 73,091,258-73,125,557 SLC29A3, LOC105378353
    nsv6890930copy number variation1nstd229human GRCh38 chr10: 71,174,318-71,658,626 , GRCh37.p13 chr10: 72,934,075-73,418,383 UNC5B, CDH23-AS1, 7 more genes
    nsv6889307copy number variation1nstd229human GRCh38 chr10: 71,357,612-71,371,193 , GRCh37.p13 chr10: 73,117,369-73,130,950 SLC29A3
    nsv6886595copy number variation1nstd229human GRCh38 chr10: 71,352,913-71,353,015 , GRCh37.p13 chr10: 73,112,670-73,112,772 SLC29A3
    nsv6884561copy number variation1nstd229human GRCh38 chr10: 71,197,245-71,475,767 , GRCh37.p13 chr10: 72,957,002-73,235,524 CDH23, LOC112268061, 5 more genes
    nsv6882746copy number variation1nstd229human GRCh38 chr10: 71,299,094-71,340,999 , GRCh37.p13 chr10: 73,058,851-73,100,756 SLC29A3, UNC5B, 1 more genes
    nsv6881758copy number variation1nstd229human GRCh38 chr10: 71,172,301-71,380,000 , GRCh37.p13 chr10: 72,932,058-73,139,757 UNC5B-AS1, LOC105378353, 3 more genes
    nsv6881377copy number variation1nstd229human GRCh38 chr10: 71,317,743-71,320,293 , GRCh37.p13 chr10: 73,077,500-73,080,050 SLC29A3
    nsv6880736copy number variation1nstd229human GRCh38 chr10: 71,209,769-71,434,423 , GRCh37.p13 chr10: 72,969,526-73,194,180 SLC29A3, CDH23, 4 more genes
    nsv6878412copy number variation1nstd229human GRCh38 chr10: 71,318,601-71,322,100 , GRCh37.p13 chr10: 73,078,358-73,081,857 SLC29A3
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