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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916897copy number variation1nstd209human GRCh38 chr11: 7,789,626-7,811,830 , GRCh37.p13 chr11: 7,811,173-7,833,377 OR5P2
    nsv5867484copy number variation1nstd209human GRCh38 chr11: 7,789,603-7,811,738 , GRCh37.p13 chr11: 7,811,150-7,833,285 OR5P2
    nsv5587456copy number variation1nstd207human GRCh38 chr11: 7,789,629-7,811,833 , GRCh37.p13 chr11: 7,811,176-7,833,380 OR5P2
    nsv5510983copy number variation1nstd206human GRCh38 chr11: 7,737,600-7,864,000 , GRCh37.p13 chr11: 7,759,147-7,885,547 OR5E1P, OR5P1P, 5 more genes
    nsv5502797copy number variation1nstd206human GRCh38 chr11: 7,789,629-7,811,831 , GRCh37.p13 chr11: 7,811,176-7,833,378 OR5P2
    nsv5500971copy number variation1nstd206human GRCh38 chr11: 7,515,650-7,976,370 , GRCh37.p13 chr11: 7,536,881-7,997,917 OR5P4P, RPL7AP55, 17 more genes
    nsv5316893copy number variation1nstd204human GRCh38.p13 chr11: 7,789,628-7,811,832 , GRCh37.p13 chr11: 7,811,175-7,833,379 OR5P2
    nsv5315802copy number variation1nstd204human GRCh38.p13 chr11: 7,790,971-7,802,530 , GRCh37.p13 chr11: 7,812,518-7,824,077 OR5P2
    nsv5250457copy number variation1nstd204human GRCh38.p13 chr11: 7,795,897-7,796,896 , GRCh37.p13 chr11: 7,817,444-7,818,443 OR5P2
    nsv5250170copy number variation1nstd204human GRCh38.p13 chr11: 7,790,423-7,799,762 , GRCh37.p13 chr11: 7,811,970-7,821,309 OR5P2
    nsv5247719copy number variation1nstd204human GRCh38.p13 chr11: 7,788,372-7,811,847 , GRCh37.p13 chr11: 7,809,919-7,833,394 OR5P2
    nsv5246710copy number variation1nstd204human GRCh38.p13 chr11: 7,789,553-7,795,458 , GRCh37.p13 chr11: 7,811,100-7,817,005 OR5P2
    nsv5245746copy number variation1nstd204human GRCh38.p13 chr11: 7,789,601-7,811,800 , GRCh37.p13 chr11: 7,811,148-7,833,347 OR5P2
    nsv4978105copy number variation1nstd200human GRCh38 chr11: 7,793,845-7,794,091 , GRCh37.p13 chr11: 7,815,392-7,815,638 OR5P2
    nsv4978104copy number variation1nstd200human GRCh38 chr11: 7,789,629-7,811,831 , GRCh37.p13 chr11: 7,811,176-7,833,378 OR5P2
    nsv4978101copy number variation1nstd200human GRCh38 chr11: 7,770,684-7,923,891 , GRCh37.p13 chr11: 7,792,231-7,945,438 OR5E1P, OR5P1P, 6 more genes
    nsv4978098copy number variation1nstd200human GRCh38 chr11: 7,756,148-7,855,558 , GRCh37.p13 chr11: 7,777,695-7,877,105 OR5E1P, OR5P1P, 4 more genes
    nsv4839968copy number variation1nstd200human GRCh37 chr11: 7,815,392-7,815,638 , GRCh38.p12 chr11|NT_187583.1: 14,713-14,959 , GRCh38.p12 chr11: 7,793,845-7,794,091 , GRCh38.p12 chr11|NW_011332695.1: 14,713-14,959 OR5P2
    nsv4839534copy number variation1nstd200human GRCh37 chr11: 7,811,176-7,833,378 , GRCh38.p12 chr11: 7,789,629-7,811,831 , GRCh38.p12 chr11|NW_011332695.1: 10,497-32,701 , GRCh38.p12 chr11|NT_187583.1: 10,497-32,699 OR5P2
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
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