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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv6733646copy number variation1nstd229human GRCh38 chr3: 170,017,641-170,101,603 , GRCh37.p13 chr3: 169,735,429-169,819,391 GPR160, PHC3, 3 more genes
    nsv6733019copy number variation1nstd229human GRCh38 chr3: 170,111,801-170,300,400 , GRCh37.p13 chr3: 169,829,589-170,018,188 RNU6-315P, PHC3, 3 more genes
    nsv6730888copy number variation1nstd229human GRCh38 chr3: 170,173,024-170,173,292 , GRCh37.p13 chr3: 169,890,812-169,891,080 PHC3
    nsv6729870copy number variation1nstd229human GRCh38 chr3: 170,084,788-170,090,125 , GRCh37.p13 chr3: 169,802,576-169,807,913 GPR160, PHC3
    nsv6729228copy number variation1nstd229human GRCh38 chr3: 170,091,147-170,092,377 , GRCh37.p13 chr3: 169,808,935-169,810,165 PHC3
    nsv6726954copy number variation1nstd229human GRCh38 chr3: 170,115,801-170,143,100 , GRCh37.p13 chr3: 169,833,589-169,860,888 PHC3, LOC105374209
    nsv6725692copy number variation1nstd229human GRCh38 chr3: 170,173,012-170,173,262 , GRCh37.p13 chr3: 169,890,800-169,891,050 PHC3
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6570195inversion1nstd223human GRCh38 chr3: 170,155,736-170,155,851 , GRCh37.p13 chr3: 169,873,524-169,873,639 PHC3
    nsv6565808inversion1nstd223human GRCh38 chr3: 170,175,973-170,177,617 , GRCh37.p13 chr3: 169,893,761-169,895,405 PHC3
    nsv6565456inversion1nstd223human GRCh38 chr3: 170,165,727-170,166,344 , GRCh37.p13 chr3: 169,883,515-169,884,132 PHC3
    nsv6564349inversion1nstd223human GRCh38 chr3: 170,152,568-170,153,448 , GRCh37.p13 chr3: 169,870,356-169,871,236 PHC3
    nsv6563213inversion1nstd223human GRCh38 chr3: 170,123,736-170,123,917 , GRCh37.p13 chr3: 169,841,524-169,841,705 PHC3
    nsv6561451inversion1nstd223human GRCh38 chr3: 170,146,284-170,146,807 , GRCh37.p13 chr3: 169,864,072-169,864,595 PHC3
    nsv6557857inversion1nstd223human GRCh38 chr3: 170,117,717-170,118,423 , GRCh37.p13 chr3: 169,835,505-169,836,211 LOC105374209, PHC3
    nsv6375571copy number variation1nstd223human GRCh38 chr3: 170,000,060-170,178,407 , GRCh37.p13 chr3: 169,717,848-169,896,195 GPR160, PHC3, 5 more genes
    nsv6370042copy number variation1nstd223human GRCh38 chr3: 170,133,464-170,135,398 , GRCh37.p13 chr3: 169,851,252-169,853,186 PHC3
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