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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068936inversion1nstd229human GRCh38 chr12: 75,617,673-76,899,935 , GRCh37.p13 chr12: 76,011,453-77,293,715 CSRP2, OSBPL8, 23 more genes
    nsv7068424inversion1nstd229human GRCh38 chr12: 75,621,086-76,899,941 , GRCh37.p13 chr12: 76,014,866-77,293,721 LOC100289143, LOC105369844, 23 more genes
    nsv6935595copy number variation1nstd229human GRCh38 chr12: 76,072,874-76,142,151 , GRCh37.p13 chr12: 76,466,654-76,535,931 LOC641695, RNU6-1271P, 1 more genes
    nsv6928212copy number variation1nstd229human GRCh38 chr12: 76,034,084-76,038,297 , GRCh37.p13 chr12: 76,427,864-76,432,077 NAP1L1
    nsv6922283copy number variation1nstd229human GRCh38 chr12: 76,057,201-76,063,100 , GRCh37.p13 chr12: 76,450,981-76,456,880 LOC100652897, NAP1L1
    nsv6920478copy number variation1nstd229human GRCh38 chr12: 76,005,476-76,062,917 , GRCh37.p13 chr12: 76,399,256-76,456,697 LOC100652897, PHLDA1, 2 more genes
    nsv6920359copy number variation1nstd229human GRCh38 chr12: 76,041,318-76,044,626 , GRCh37.p13 chr12: 76,435,098-76,438,406 NAP1L1
    nsv6919972copy number variation1nstd229human GRCh38 chr12: 76,069,665-76,070,005 , GRCh37.p13 chr12: 76,463,445-76,463,785 NAP1L1
    nsv6587098inversion1nstd223human GRCh38 chr12: 70,939,082-79,478,721 , GRCh37.p13 chr12: 71,332,862-79,872,501 , H3P35, 83 more genes
    nsv6473489copy number variation1nstd223human GRCh38 chr12: 76,041,318-76,044,625 , GRCh37.p13 chr12: 76,435,098-76,438,405 NAP1L1
    nsv6469911copy number variation1nstd223human GRCh38 chr12: 76,044,601-76,045,600 , GRCh37.p13 chr12: 76,438,381-76,439,380 NAP1L1
    nsv6464898copy number variation1nstd223human GRCh38 chr12: 76,072,442-76,073,868 , GRCh37.p13 chr12: 76,466,222-76,467,648 NAP1L1
    nsv6462166copy number variation1nstd223human GRCh38 chr12: 76,065,083-76,065,536 , GRCh37.p13 chr12: 76,458,863-76,459,316 NAP1L1
    nsv6457426copy number variation1nstd223human GRCh38 chr12: 76,077,202-76,077,701 , GRCh37.p13 chr12: 76,470,982-76,471,481 NAP1L1
    nsv6455602copy number variation1nstd223human GRCh38 chr12: 76,044,401-76,046,600 , GRCh37.p13 chr12: 76,438,181-76,440,380 NAP1L1
    nsv6291127copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,084,476-77,065,764 , GRCh38.p12 chr12: 69,690,696-76,671,984 LOC100130268, RNU6-1012P, 78 more genes
    nsv6199406copy number variation1nstd214human GRCh38 chr12: 76,051,562-76,051,702 , GRCh37.p13 chr12: 76,445,342-76,445,482 NAP1L1
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132437copy number variation1nstd213human GRCh37 chr12: 75,550,000-78,060,001 , GRCh38.p12 chr12: 75,156,220-77,666,221 , CSRP2, 40 more genes
    nsv5946943copy number variation1nstd209human GRCh38 chr12: 76,035,071-76,035,282 , GRCh37.p13 chr12: 76,428,851-76,429,062 NAP1L1
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