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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6877156copy number variation1nstd229human GRCh38 chr9: 120,543,841-120,873,244 , GRCh37.p13 chr9: 123,306,119-123,635,522 AHCYP2, FBXW2, 6 more genes
    nsv6873124copy number variation1nstd229human GRCh38 chr9: 120,877,491-120,879,434 , GRCh37.p13 chr9: 123,639,769-123,641,712 PHF19
    nsv6869795copy number variation1nstd229human GRCh38 chr9: 120,864,301-120,913,700 , GRCh37.p13 chr9: 123,626,579-123,675,978 PHF19, TRAF1
    nsv6869112copy number variation1nstd229human GRCh38 chr9: 120,878,252-120,881,331 , GRCh37.p13 chr9: 123,640,530-123,643,609 PHF19
    nsv6863632copy number variation1nstd229human GRCh38 chr9: 120,896,210-120,896,270 , GRCh37.p13 chr9: 123,658,488-123,658,548 PHF19
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6443612copy number variation1nstd223human GRCh38 chr9: 120,889,726-120,891,748 , GRCh37.p13 chr9: 123,652,004-123,654,026 PHF19
    nsv6435917copy number variation1nstd223human GRCh38 chr9: 120,897,175-120,906,917 , GRCh37.p13 chr9: 123,659,453-123,669,195 PHF19, TRAF1
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137053copy number variation1nstd213human GRCh37 chr9: 123,580,000-123,920,001 , GRCh38.p12 chr9: 120,817,722-121,157,723 C5, PSMD5, 5 more genes
    nsv6137052copy number variation1nstd213human GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722 MEGF9, GGTA1, 61 more genes
    nsv5638580insertion1nstd207human GRCh38 chr9: 120,870,766-120,870,766 , GRCh37.p13 chr9: 123,633,044-123,633,044 PHF19
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983498copy number variation1nstd200human GRCh38 chr9: 120,871,019-120,871,865 , GRCh37.p13 chr9: 123,633,297-123,634,143 PHF19
    nsv4835071copy number variation1nstd200human GRCh37 chr9: 123,633,297-123,634,143 , GRCh38.p12 chr9: 120,871,019-120,871,865 PHF19
    nsv4830416copy number variation1nstd200human GRCh37 chr9: 123,596,208-123,617,768 , GRCh38.p12 chr9: 120,833,930-120,855,490 PHF19, PSMD5, 1 more genes
    nsv4493376mobile element insertion1nstd166human GRCh37.p13 chr9: 123,628,946-123,628,946 , GRCh38.p12 chr9: 120,866,668-120,866,668 PHF19
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