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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125611copy number variation1nstd186human GRCh37 chr16: 89,799,182-89,799,480 , GRCh38.p12 chr16: 89,732,774-89,733,072 ZNF276
    nsv6112808copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,620,873-89,881,041 , GRCh38.p12 chr16: 89,554,465-89,814,633 CHMP1A, CDK10, 12 more genes
    nsv5946711copy number variation1nstd209human GRCh38 chr16: 89,610,799-89,855,128 , GRCh37.p13 chr16: 89,677,207-89,921,536 , CDK10, 11 more genes
    nsv5934298copy number variation1nstd209human GRCh38 chr16: 89,728,655-89,728,789 , GRCh37.p13 chr16: 89,795,063-89,795,197 ZNF276
    nsv5672942copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,807,202-89,883,024 , GRCh38.p12 chr16: 89,740,794-89,816,616 ZNF276, FANCA
    nsv5672940copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 89,804,999-89,871,810 , GRCh38.p12 chr16: 89,738,591-89,805,402 FANCA, ZNF276
    nsv5672854copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,804,999-89,825,128 , GRCh38.p12 chr16: 89,738,591-89,758,720 ZNF276, FANCA
    nsv5603127copy number variation1nstd207human GRCh38 chr16: 89,732,723-89,732,998 , GRCh37.p13 chr16: 89,799,131-89,799,406 ZNF276
    nsv5527155copy number variation1nstd206human GRCh38 chr16: 89,736,711-89,737,055 , GRCh37.p13 chr16: 89,803,119-89,803,463 FANCA, ZNF276
    nsv5515569copy number variation1nstd206human GRCh38 chr16: 89,732,734-89,733,113 , GRCh37.p13 chr16: 89,799,142-89,799,521 ZNF276
    nsv5390413copy number variation1nstd186human GRCh37 chr16: 89,799,132-89,799,419 , GRCh38.p12 chr16: 89,732,724-89,733,011 ZNF276
    nsv5380862copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,805,009-89,858,965 , GRCh38.p12 chr16: 89,738,601-89,792,557 FANCA, ZNF276
    nsv5318231copy number variation1nstd204human GRCh38.p13 chr16: 89,724,120-89,727,556 , GRCh37.p13 chr16: 89,790,528-89,793,964 ZNF276
    nsv5305622copy number variation1nstd204human GRCh38.p13 chr16: 89,732,536-89,733,215 , GRCh37.p13 chr16: 89,798,944-89,799,623 ZNF276
    nsv5292585copy number variation1nstd204human GRCh38.p13 chr16: 89,732,701-89,732,900 , GRCh37.p13 chr16: 89,799,109-89,799,308 ZNF276
    nsv5291075copy number variation1nstd204human GRCh38.p13 chr16: 89,281,101-89,907,300 , GRCh37.p13 chr16: 89,347,509-89,973,708 , SPATA33, 25 more genes
    nsv5015139copy number variation1nstd200human GRCh38 chr16: 89,726,414-89,754,520 , GRCh37.p13 chr16: 89,792,822-89,820,928 ZNF276, FANCA
    nsv5015138copy number variation1nstd200human GRCh38 chr16: 89,719,292-89,734,057 , GRCh37.p13 chr16: 89,785,700-89,800,465 VPS9D1, ZNF276
    nsv5015136copy number variation1nstd200human GRCh38 chr16: 89,684,263-89,734,359 , GRCh37.p13 chr16: 89,750,671-89,800,767 CDK10, VPS9D1, 4 more genes
    nsv5015122copy number variation1nstd200human GRCh38 chr16: 89,610,886-89,721,603 , GRCh37.p13 chr16: 89,677,294-89,788,011 DPEP1, CHMP1A, 7 more genes
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