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Items: 1 to 20 of 153

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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
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv6897733copy number variation1nstd229human GRCh38 chr10: 14,809,152-14,886,833 , GRCh37.p13 chr10: 14,851,151-14,928,832 SUV39H2, CDNF, 2 more genes
    nsv6893098copy number variation1nstd229human GRCh38 chr10: 14,894,360-14,894,678 , GRCh37.p13 chr10: 14,936,359-14,936,677 SUV39H2
    nsv6886215copy number variation1nstd229human GRCh38 chr10: 14,892,072-14,892,177 , GRCh37.p13 chr10: 14,934,071-14,934,176 SUV39H2
    nsv6449412copy number variation1nstd223human GRCh38 chr10: 14,876,917-14,877,435 , GRCh37.p13 chr10: 14,918,916-14,919,434 SUV39H2
    nsv6435771copy number variation1nstd223human GRCh38 chr10: 14,894,360-14,894,666 , GRCh37.p13 chr10: 14,936,359-14,936,665 SUV39H2
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 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
    nsv6240417mobile element insertion1nstd215human GRCh38 chr10: 14,897,734-14,897,734 , GRCh37.p13 chr10: 14,939,733-14,939,733 SUV39H2, DCLRE1C
    nsv6142361copy number variation1nstd206human GRCh38 chr10: 14,894,340-14,894,686 , GRCh37.p13 chr10: 14,936,339-14,936,685 SUV39H2
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv6112737copy number variation1nstd102humannot provided GRCh37 chr10: 14,945,105-14,954,010 , GRCh38.p12 chr10: 14,903,106-14,912,011 DCLRE1C, SUV39H2
    nsv6005774copy number variation1nstd212human GRCh38 chr10: 14,894,349-14,894,666 , GRCh37.p13 chr10: 14,936,348-14,936,665 SUV39H2
    nsv5925013copy number variation1nstd209human GRCh38 chr10: 14,894,349-14,894,665 , GRCh37.p13 chr10: 14,936,348-14,936,664 SUV39H2
    nsv5909262copy number variation1nstd209human GRCh38 chr10: 14,877,148-14,877,199 , GRCh37.p13 chr10: 14,919,147-14,919,198 SUV39H2
    nsv5723122mobile element insertion1nstd211human GRCh38 chr10: 14,878,192-14,878,192 , GRCh37.p13 chr10: 14,920,191-14,920,191 SUV39H2
    nsv5672529copy number variation1nstd102humanPathogenic GRCh37 chr10: 14,946,600-14,951,339 , GRCh38.p12 chr10: 14,904,601-14,909,340 DCLRE1C, SUV39H2
    nsv5602851copy number variation1nstd207human GRCh38 chr10: 14,894,349-14,894,665 , GRCh37.p13 chr10: 14,936,348-14,936,664 SUV39H2
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