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Items: 1 to 20 of 843

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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
    nsv7075489inversion1nstd229human GRCh38 chr10: 35,569,842-35,569,893 , GRCh37.p13 chr10: 35,858,770-35,858,821 CCNY
    nsv7067479inversion1nstd229human GRCh38 chr10: 34,842,900-35,440,966 , GRCh37.p13 chr10: 35,131,828-35,729,894 LINC02634, PRDX2P2, 13 more genes
    nsv7065802inversion1nstd229human GRCh38 chr10: 35,090,475-35,277,204 , GRCh37.p13 chr10: 35,379,403-35,566,132 CREM, CUL2, 6 more genes
    nsv7065010inversion1nstd229human GRCh38 chr10: 32,699,822-35,479,064 , GRCh37.p13 chr10: 32,988,750-35,767,992 RNU6-1167P, MIR3611, 34 more genes
    nsv7064321inversion1nstd229human GRCh38 chr10: 34,888,952-35,327,837 , GRCh37.p13 chr10: 35,177,880-35,616,765 LINC02634, RNU6-847P, 12 more genes
    nsv7059585inversion1nstd229human GRCh38 chr10: 35,451,886-35,451,929 , GRCh37.p13 chr10: 35,740,814-35,740,857 CCNY
    nsv7058248inversion1nstd229human GRCh38 chr10: 34,955,235-35,365,379 , GRCh37.p13 chr10: 35,244,163-35,654,307 LINC02634, MIR3611, 10 more genes
    nsv6897922copy number variation1nstd229human GRCh38 chr10: 35,456,011-35,458,750 , GRCh37.p13 chr10: 35,744,939-35,747,678 CCNY
    nsv6897867copy number variation1nstd229human GRCh38 chr10: 35,238,836-35,248,088 , GRCh37.p13 chr10: 35,527,764-35,537,016 LINC02634, CCNY
    nsv6897330copy number variation1nstd229human GRCh38 chr10: 35,373,808-35,373,903 , GRCh37.p13 chr10: 35,662,736-35,662,831 CCNY
    nsv6897014copy number variation1nstd229human GRCh38 chr10: 35,275,336-35,277,449 , GRCh37.p13 chr10: 35,564,264-35,566,377 CCNY
    nsv6896180copy number variation1nstd229human GRCh38 chr10: 35,433,323-35,440,588 , GRCh37.p13 chr10: 35,722,251-35,729,516 CCNY
    nsv6895870copy number variation1nstd229human GRCh38 chr10: 35,487,901-35,502,000 , GRCh37.p13 chr10: 35,776,829-35,790,928 CCNY
    nsv6895606copy number variation1nstd229human GRCh38 chr10: 35,322,620-35,365,145 , GRCh37.p13 chr10: 35,611,548-35,654,073 CCNY
    nsv6895412copy number variation1nstd229human GRCh38 chr10: 35,438,401-35,440,500 , GRCh37.p13 chr10: 35,727,329-35,729,428 CCNY
    nsv6894836copy number variation1nstd229human GRCh38 chr10: 35,115,433-35,301,857 , GRCh37.p13 chr10: 35,404,361-35,590,785 ATP6V1G1P4, LOC107984220, 7 more genes
    nsv6894512copy number variation1nstd229human GRCh38 chr10: 35,393,107-35,394,158 , GRCh37.p13 chr10: 35,682,035-35,683,086 CCNY
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
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