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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7147520insertion1nstd232human GRCh37.p13 chr7: 11,091,408-11,091,408 , GRCh38.p12 chr7: 11,051,781-11,051,781 PHF14
    nsv7056553inversion1nstd229human GRCh38 chr7: 10,976,854-10,990,332 , GRCh37.p13 chr7: 11,016,481-11,029,959 PHF14
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7053877inversion1nstd229human GRCh38 chr7: 11,112,113-11,119,091 , GRCh37.p13 chr7: 11,151,740-11,158,718 PHF14
    nsv7050340inversion1nstd229human GRCh38 chr7: 10,989,812-10,992,500 , GRCh37.p13 chr7: 11,029,439-11,032,127 PHF14
    nsv7050015inversion1nstd229human GRCh38 chr7: 11,039,525-11,045,488 , GRCh37.p13 chr7: 11,079,152-11,085,115 PHF14
    nsv7049984inversion1nstd229human GRCh38 chr7: 11,159,456-12,799,960 , GRCh37.p13 chr7: 11,199,083-12,839,585 THSD7A, LOC105375156, 17 more genes
    nsv7040409inversion1nstd229human GRCh38 chr7: 11,034,082-11,149,546 , GRCh37.p13 chr7: 11,073,709-11,189,173 PHF14
    nsv6817896copy number variation1nstd229human GRCh38 chr7: 10,982,819-10,986,020 , GRCh37.p13 chr7: 11,022,446-11,025,647 PHF14
    nsv6817374copy number variation1nstd229human GRCh38 chr7: 10,753,988-11,038,567 , GRCh37.p13 chr7: 10,793,615-11,078,194 PHF14, MGC4859, 3 more genes
    nsv6816205copy number variation1nstd229human GRCh38 chr7: 11,000,201-11,009,200 , GRCh37.p13 chr7: 11,039,828-11,048,827 RPL23AP52, PHF14
    nsv6814932copy number variation1nstd229human GRCh38 chr7: 11,162,480-11,163,909 , GRCh37.p13 chr7: 11,202,107-11,203,536 PHF14
    nsv6814186copy number variation1nstd229human GRCh38 chr7: 10,823,305-11,529,482 , GRCh37.p13 chr7: 10,862,932-11,569,109 PHF14, THSD7A, 4 more genes
    nsv6812939copy number variation1nstd229human GRCh38 chr7: 11,129,201-11,134,300 , GRCh37.p13 chr7: 11,168,828-11,173,927 PHF14
    nsv6812841copy number variation1nstd229human GRCh38 chr7: 11,121,068-11,155,965 , GRCh37.p13 chr7: 11,160,695-11,195,592 PHF14
    nsv6812410copy number variation1nstd229human GRCh38 chr7: 11,157,033-11,438,467 , GRCh37.p13 chr7: 11,196,660-11,478,094 PHF14, NPM1P11, 1 more genes
    nsv6811597copy number variation1nstd229human GRCh38 chr7: 11,080,786-11,098,465 , GRCh37.p13 chr7: 11,120,413-11,138,092 PHF14
    nsv6810848copy number variation1nstd229human GRCh38 chr7: 11,111,435-11,113,678 , GRCh37.p13 chr7: 11,151,062-11,153,305 PHF14
    nsv6808852copy number variation1nstd229human GRCh38 chr7: 10,975,598-10,981,789 , GRCh37.p13 chr7: 11,015,225-11,021,416 PHF14
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