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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972064insertion1nstd209human GRCh38 chr16: 31,909,080-31,909,080 , GRCh37.p13 chr16: 31,920,401-31,920,401 ZNF267
    nsv5933296copy number variation1nstd209human GRCh38 chr16: 31,883,258-31,883,326 , GRCh37.p13 chr16: 31,894,579-31,894,647 ZNF267
    nsv5930751copy number variation1nstd209human GRCh38 chr16: 31,910,157-31,912,943 , GRCh37.p13 chr16: 31,921,478-31,924,264 ZNF267
    nsv5884587copy number variation1nstd209human GRCh38 chr16: 31,910,181-31,912,980 , GRCh37.p13 chr16: 31,921,502-31,924,301 ZNF267
    nsv5587511copy number variation1nstd207human GRCh38 chr16: 31,910,157-31,912,943 , GRCh37.p13 chr16: 31,921,478-31,924,264 ZNF267
    nsv5527535copy number variation1nstd206human GRCh38 chr16: 31,914,968-31,915,049 , GRCh37.p13 chr16: 31,926,289-31,926,370 ZNF267
    nsv5515915copy number variation1nstd206human GRCh38 chr16: 31,910,160-31,912,944 , GRCh37.p13 chr16: 31,921,481-31,924,265 ZNF267
    nsv5313381copy number variation1nstd204human GRCh38.p13 chr16: 31,910,150-31,912,953 , GRCh37.p13 chr16: 31,921,471-31,924,274 ZNF267
    nsv5301051copy number variation1nstd204human GRCh38.p13 chr16: 31,854,272-34,660,717 , GRCh37.p13 chr16: 31,865,593-34,023,151 , BCAP31P2, 80 more genes
    nsv5003547copy number variation1nstd200human GRCh38 chr16: 31,910,160-31,912,944 , GRCh37.p13 chr16: 31,921,481-31,924,265 ZNF267
    nsv5003546copy number variation1nstd200human GRCh38 chr16: 31,880,550-31,882,221 , GRCh37.p13 chr16: 31,891,871-31,893,542 ZNF267
    nsv4856857copy number variation1nstd200human GRCh37 chr16: 31,921,481-31,924,265 , GRCh38.p12 chr16: 31,910,160-31,912,944 ZNF267
    nsv4856856copy number variation1nstd200human GRCh37 chr16: 31,916,712-31,919,086 , GRCh38.p12 chr16: 31,905,391-31,907,765 ZNF267
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4669516copy number variation1nstd186human GRCh37 chr16: 31,921,501-31,924,157 , GRCh38.p12 chr16: 31,910,180-31,912,836 ZNF267
    nsv4669119copy number variation1nstd186human GRCh37 chr16: 31,921,478-31,924,265 , GRCh38.p12 chr16: 31,910,157-31,912,944 ZNF267
    nsv4651790copy number variation4nstd186human GRCh37 chr16: 31,921,481-31,924,265 , GRCh38.p12 chr16: 31,910,160-31,912,944 ZNF267
    nsv4646154copy number variation1nstd186human GRCh37 chr16: 31,921,463-31,924,290 , GRCh38.p12 chr16: 31,910,142-31,912,969 ZNF267
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