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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
    nsv7093788copy number variation1nstd102humanUncertain significance GRCh37 chr10: 30,602,538-31,816,192 , GRCh38.p12 chr10: 30,313,609-31,527,264 LOC100505502, HNRNPA1P32, 24 more genes
    nsv7073369inversion1nstd229human GRCh38 chr10: 30,996,703-31,002,088 , GRCh37.p13 chr10: 31,285,632-31,291,017 ZNF438
    nsv7072543inversion1nstd229human GRCh38 chr10: 30,996,122-30,996,145 , GRCh37.p13 chr10: 31,285,051-31,285,074 ZNF438
    nsv6897950copy number variation1nstd229human GRCh38 chr10: 30,857,985-30,861,689 , GRCh37.p13 chr10: 31,146,914-31,150,618 ZNF438
    nsv6897864copy number variation1nstd229human GRCh38 chr10: 30,839,815-30,933,933 , GRCh37.p13 chr10: 31,128,744-31,222,862 DDX10P1, ZNF438
    nsv6895492copy number variation1nstd229human GRCh38 chr10: 30,867,368-30,873,501 , GRCh37.p13 chr10: 31,156,297-31,162,430 ZNF438
    nsv6895163copy number variation1nstd229human GRCh38 chr10: 30,976,101-30,983,700 , GRCh37.p13 chr10: 31,265,030-31,272,629 ZNF438
    nsv6895061copy number variation1nstd229human GRCh38 chr10: 30,863,052-30,863,087 , GRCh37.p13 chr10: 31,151,981-31,152,016 ZNF438
    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
    nsv6893195copy number variation1nstd229human GRCh38 chr10: 30,957,801-30,962,900 , GRCh37.p13 chr10: 31,246,730-31,251,829 ZNF438
    nsv6891987copy number variation1nstd229human GRCh38 chr10: 30,851,837-30,855,444 , GRCh37.p13 chr10: 31,140,766-31,144,373 ZNF438
    nsv6891363copy number variation1nstd229human GRCh38 chr10: 30,901,754-30,907,169 , GRCh37.p13 chr10: 31,190,683-31,196,098 ZNF438
    nsv6886621copy number variation1nstd229human GRCh38 chr10: 30,885,803-30,926,610 , GRCh37.p13 chr10: 31,174,732-31,215,539 DDX10P1, ZNF438
    nsv6885964copy number variation1nstd229human GRCh38 chr10: 30,980,434-30,986,690 , GRCh37.p13 chr10: 31,269,363-31,275,619 ZNF438
    nsv6885728copy number variation1nstd229human GRCh38 chr10: 30,924,737-30,926,852 , GRCh37.p13 chr10: 31,213,666-31,215,781 ZNF438
    nsv6885593copy number variation1nstd229human GRCh38 chr10: 30,945,301-30,985,200 , GRCh37.p13 chr10: 31,234,230-31,274,129 ZNF438
    nsv6883998copy number variation1nstd229human GRCh38 chr10: 30,865,059-31,283,011 , GRCh37.p13 chr10: 31,153,988-31,571,940 ZNF438, DDX10P1, 5 more genes
    nsv6882294copy number variation1nstd229human GRCh38 chr10: 30,893,616-30,896,638 , GRCh37.p13 chr10: 31,182,545-31,185,567 ZNF438
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