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Items: 1 to 20 of 962

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076151inversion1nstd229human GRCh38 chr22: 28,223,242-28,335,530 , GRCh37.p13 chr22: 28,619,230-28,731,518 TTC28
    nsv7073174inversion1nstd229human GRCh38 chr22: 28,238,760-28,242,357 , GRCh37.p13 chr22: 28,634,748-28,638,345 TTC28
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7067376inversion1nstd229human GRCh38 chr22: 28,295,094-28,295,153 , GRCh37.p13 chr22: 28,691,082-28,691,141 TTC28
    nsv7065634inversion1nstd229human GRCh38 chr22: 28,530,209-28,549,533 , GRCh37.p13 chr22: 28,926,197-28,945,521 LOC101929594, TTC28
    nsv7063702inversion1nstd229human GRCh38 chr22: 28,242,468-28,247,298 , GRCh37.p13 chr22: 28,638,456-28,643,286 TTC28
    nsv7062494inversion1nstd229human GRCh38 chr22: 28,246,723-28,250,616 , GRCh37.p13 chr22: 28,642,711-28,646,604 TTC28
    nsv7060134inversion1nstd229human GRCh38 chr22: 28,460,285-28,462,882 , GRCh37.p13 chr22: 28,856,273-28,858,870 TTC28, MIR5739
    nsv7058113inversion1nstd229human GRCh38 chr22: 28,545,359-28,549,225 , GRCh37.p13 chr22: 28,941,347-28,945,213 TTC28, LOC101929594
    nsv7037590copy number variation1nstd229human GRCh38 chr22: 28,393,540-28,393,891 , GRCh37.p13 chr22: 28,789,528-28,789,879 TTC28
    nsv7036973copy number variation1nstd229human GRCh38 chr22: 28,571,902-28,589,910 , GRCh37.p13 chr22: 28,967,890-28,985,898 TTC28
    nsv7036378copy number variation1nstd229human GRCh38 chr22: 28,386,805-28,388,881 , GRCh37.p13 chr22: 28,782,793-28,784,869 TTC28
    nsv7036142copy number variation1nstd229human GRCh38 chr22: 28,127,569-28,136,963 , GRCh37.p13 chr22: 28,523,557-28,532,951 TTC28
    nsv7035945copy number variation1nstd229human GRCh38 chr22: 27,971,053-27,987,888 , GRCh37.p13 chr22: 28,367,041-28,383,876 TTC28-AS1, TTC28
    nsv7035424copy number variation1nstd229human GRCh38 chr22: 28,251,712-28,267,075 , GRCh37.p13 chr22: 28,647,700-28,663,063 TTC28
    nsv7035117copy number variation1nstd229human GRCh38 chr22: 28,613,077-28,618,912 , GRCh37.p13 chr22: 29,009,065-29,014,900 TTC28
    nsv7035038copy number variation1nstd229human GRCh38 chr22: 28,129,168-28,141,416 , GRCh37.p13 chr22: 28,525,156-28,537,404 TTC28
    nsv7034892copy number variation1nstd229human GRCh38 chr22: 28,151,805-28,157,525 , GRCh37.p13 chr22: 28,547,793-28,553,513 TTC28
    nsv7034689copy number variation1nstd229human GRCh38 chr22: 28,404,663-28,693,104 , GRCh37.p13 chr22: 28,800,651-29,089,092 RN7SL162P, LOC101929594, 3 more genes
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