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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
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7147439insertion1nstd232human GRCh37.p13 chr6: 167,198,133-167,198,133 , GRCh38.p12 chr6: 166,784,645-166,784,645 RPS6KA2
    nsv7143856copy number variation1nstd232human GRCh37.p13 chr6: 167,061,283-167,061,366 , GRCh38.p12 chr6: 166,647,795-166,647,878 RPS6KA2, LOC107986671
    nsv7138746copy number variation1nstd232human GRCh37.p13 chr6: 167,197,275-167,197,337 , GRCh38.p12 chr6: 166,783,787-166,783,849 RPS6KA2
    nsv7138031copy number variation1nstd232human GRCh37.p13 chr6: 167,272,485-167,272,545 , GRCh38.p12 chr6: 166,858,997-166,859,057 RPS6KA2
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7052454inversion1nstd229human GRCh38 chr6: 166,589,743-166,589,822 , GRCh37.p13 chr6: 167,003,231-167,003,310 RPS6KA2
    nsv7050240inversion1nstd229human GRCh38 chr6: 166,688,906-166,693,748 , GRCh37.p13 chr6: 167,102,394-167,107,236 RPS6KA2
    nsv7040994inversion1nstd229human GRCh38 chr6: 166,501,412-166,511,056 , GRCh37.p13 chr6: 166,914,900-166,924,544 RPS6KA2, MIR1913
    nsv7039326inversion1nstd229human GRCh38 chr6: 166,693,599-166,697,456 , GRCh37.p13 chr6: 167,107,087-167,110,944 RPS6KA2, LOC645468
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv6817978copy number variation1nstd229human GRCh38 chr6: 166,552,616-166,555,177 , GRCh37.p13 chr6: 166,966,104-166,968,665 RPS6KA2
    nsv6817887copy number variation1nstd229human GRCh38 chr6: 166,720,946-166,724,821 , GRCh37.p13 chr6: 167,134,434-167,138,309 RPS6KA2
    nsv6817121copy number variation1nstd229human GRCh38 chr6: 166,471,231-166,471,934 , GRCh37.p13 chr6: 166,884,719-166,885,422 RPS6KA2
    nsv6816043copy number variation1nstd229human GRCh38 chr6: 165,919,144-166,571,192 , GRCh37.p13 chr6: 166,332,632-166,984,680 HNRNPA1P49, MIR1913, 19 more genes
    nsv6815223copy number variation1nstd229human GRCh38 chr6: 166,838,746-166,838,923 , GRCh37.p13 chr6: 167,252,234-167,252,411 RPS6KA2
    nsv6815212copy number variation1nstd229human GRCh38 chr6: 166,555,414-166,555,515 , GRCh37.p13 chr6: 166,968,902-166,969,003 RPS6KA2
    nsv6815118copy number variation1nstd229human GRCh38 chr6: 166,437,783-166,437,839 , GRCh37.p13 chr6: 166,851,271-166,851,327 RPS6KA2
    nsv6814448copy number variation1nstd229human GRCh38 chr6: 166,733,543-166,745,587 , GRCh37.p13 chr6: 167,147,031-167,159,075 RPS6KA2
    nsv6814299copy number variation1nstd229human GRCh38 chr6: 166,681,035-166,681,071 , GRCh37.p13 chr6: 167,094,523-167,094,559 RPS6KA2
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