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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137781copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 59,934,593-59,940,644 , GRCh38.p12 chr17: 61,857,232-61,863,283 BRIP1
    nsv6123425copy number variation1nstd186human GRCh37 chr17: 59,868,757-59,868,874 , GRCh38.p12 chr17: 61,791,396-61,791,513 BRIP1
    nsv5947507copy number variation1nstd209human GRCh38 chr17: 61,727,424-61,727,981 , GRCh37.p13 chr17: 59,804,785-59,805,342 BRIP1
    nsv5944192copy number variation1nstd209human GRCh38 chr17: 61,789,032-61,791,460 , GRCh37.p13 chr17: 59,866,393-59,868,821 BRIP1
    nsv5941341copy number variation1nstd209human GRCh38 chr17: 61,791,396-61,791,512 , GRCh37.p13 chr17: 59,868,757-59,868,873 BRIP1
    nsv5937859copy number variation1nstd209human GRCh38 chr17: 61,740,577-61,744,203 , GRCh37.p13 chr17: 59,817,938-59,821,564 BRIP1
    nsv5877296copy number variation1nstd209human GRCh38 chr17: 61,789,080-61,791,079 , GRCh37.p13 chr17: 59,866,441-59,868,440 BRIP1
    nsv5876022copy number variation1nstd209human GRCh38 chr17: 61,783,294-61,784,593 , GRCh37.p13 chr17: 59,860,655-59,861,954 BRIP1
    nsv5873233copy number variation2nstd209human GRCh38 chr17: 61,740,689-61,742,788 , GRCh37.p13 chr17: 59,818,050-59,820,149 BRIP1
    nsv5704560mobile element insertion2nstd211human GRCh38 chr17: 61,721,636-61,721,636 , GRCh37.p13 chr17: 59,798,997-59,798,997 BRIP1
    nsv5699422mobile element insertion2nstd211human GRCh38 chr17: 61,813,270-61,813,270 , GRCh37.p13 chr17: 59,890,631-59,890,631 BRIP1
    nsv5674268insertion1nstd102humanPathogenic GRCh37 chr17: 59,926,491-59,926,491 , GRCh38 chr17: 61,849,130-61,849,130 BRIP1
    nsv5673138copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 59,924,456-59,926,623 , GRCh38.p12 chr17: 61,847,095-61,849,262 BRIP1
    nsv5673137copy number variation1nstd102humanPathogenic GRCh37 chr17: 59,770,781-59,938,900 , GRCh38.p12 chr17: 61,693,420-61,861,539 BRIP1
    nsv5673051copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 59,878,604-59,878,845 , GRCh38.p12 chr17: 61,801,243-61,801,484 BRIP1
    nsv5673050copy number variation1nstd102humanPathogenic GRCh37 chr17: 59,861,621-59,861,795 , GRCh38.p12 chr17: 61,784,260-61,784,434 BRIP1
    nsv5673049copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr17: 59,858,191-59,858,864 , GRCh38.p12 chr17: 61,780,830-61,781,503 BRIP1
    nsv5673048copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 59,770,785-59,770,879 , GRCh38.p12 chr17: 61,693,424-61,693,518 BRIP1
    nsv5672984copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 59,878,633-59,883,057 , GRCh38.p12 chr17: 61,801,272-61,805,696 BRIP1
    nsv5672890copy number variation1nstd102humanPathogenic GRCh37 chr17: 59,926,480-59,934,602 , GRCh38.p12 chr17: 61,849,119-61,857,241 BRIP1
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