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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
    nsv7065499inversion1nstd229human GRCh38 chr10: 35,933,937-37,620,453 , GRCh37.p13 chr10: 36,222,865-37,909,381 MTND1P18, LINC00993, 19 more genes
    nsv6896189copy number variation1nstd229human GRCh38 chr10: 37,321,312-37,332,318 , GRCh37.p13 chr10: 37,610,240-37,621,246 LINC00993
    nsv6893464copy number variation1nstd229human GRCh38 chr10: 37,321,651-37,330,225 , GRCh37.p13 chr10: 37,610,579-37,619,153 LINC00993
    nsv6893253copy number variation1nstd229human GRCh38 chr10: 37,334,801-37,351,700 , GRCh37.p13 chr10: 37,623,729-37,640,628 TMEM161BP1, LINC00993, 1 more genes
    nsv6883989copy number variation1nstd229human GRCh38 chr10: 36,906,541-37,474,418 , GRCh37.p13 chr10: 37,195,469-37,763,346 LOC105376497, LOC107984223, 11 more genes
    nsv6882599copy number variation1nstd229human GRCh38 chr10: 37,324,543-37,333,100 , GRCh37.p13 chr10: 37,613,471-37,622,028 LINC00993
    nsv6882543copy number variation1nstd229human GRCh38 chr10: 37,335,259-37,335,400 , GRCh37.p13 chr10: 37,624,187-37,624,328 LINC00993
    nsv6580304inversion1nstd223human GRCh38 chr10: 37,330,868-37,330,942 , GRCh37.p13 chr10: 37,619,796-37,619,870 LINC00993
    nsv6444065copy number variation1nstd223human GRCh38 chr10: 37,334,829-37,351,639 , GRCh37.p13 chr10: 37,623,757-37,640,567 TMEM161BP1, LINC00993, 1 more genes
    nsv6442616copy number variation1nstd223human GRCh38 chr10: 37,331,006-37,332,265 , GRCh37.p13 chr10: 37,619,934-37,621,193 LINC00993
    nsv6438673copy number variation1nstd223human GRCh38 chr10: 37,221,379-37,385,776 , GRCh37.p13 chr10: 37,510,307-37,674,704 ANKRD30A, TMEM161BP1, 5 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6240589mobile element insertion1nstd215human GRCh38 chr10: 37,312,321-37,312,321 , GRCh37.p13 chr10: 37,601,249-37,601,249 LINC00993
    nsv6225137insertion1nstd214human GRCh38 chr10: 37,335,297-37,335,297 , GRCh37.p13 chr10: 37,624,225-37,624,225 LINC00993
    nsv6131955copy number variation1nstd213human GRCh37 chr10: 35,740,000-38,240,001 , GRCh38.p12 chr10: 35,451,072-37,951,073 CCNY, RPL7P37, 35 more genes
    nsv6131871copy number variation1nstd213human GRCh37 chr10: 37,360,000-37,990,001 , GRCh38.p12 chr10: 37,071,072-37,701,073 TMEM161BP1, MTND1P18, 13 more genes
    nsv6088237insertion1nstd212human GRCh38 chr10: 37,346,056-37,346,056 , GRCh37.p13 chr10: 37,634,984-37,634,984 LINC00993
    nsv6082811insertion2nstd212human GRCh38 chr10: 37,330,951-37,330,951 , GRCh37.p13 chr10: 37,619,879-37,619,879 LINC00993
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