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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6979367copy number variation1nstd229human GRCh38 chr16: 30,780,442-30,780,602 , GRCh37.p13 chr16: 30,791,763-30,791,923 ZNF629, RNF40
    esv1006336insertion1estd180human NCBI36 chr16: 30,704,715-30,704,715 , GRCh37.p13 chr16: 30,797,214-30,797,214 , GRCh38.p12 chr16: 30,785,893-30,785,893 ZNF629, RNF40
    esv1725687insertion1estd22human NCBI36 chr16: 30,704,716-30,704,716 , GRCh37.p13 chr16: 30,797,215-30,797,215 , GRCh38.p12 chr16: 30,785,894-30,785,894 ZNF629, RNF40
    nsv99512insertion1nstd6human NCBI35 chr16: 30,704,707-30,704,707 , GRCh37.p13 chr16: 30,797,206-30,797,206 , GRCh38.p12 chr16: 30,785,885-30,785,885 ZNF629, RNF40
    nsv99202insertion1nstd6human NCBI35 chr16: 30,704,709-30,704,709 , GRCh37.p13 chr16: 30,797,208-30,797,208 , GRCh38.p12 chr16: 30,785,887-30,785,887 ZNF629, RNF40
    nsv1826985short tandem repeat8nstd128human GRCh37 chr16: 30,797,181-30,797,215 , GRCh38.p12 chr16: 30,785,860-30,785,894 ZNF629, RNF40
    nsv1827672short tandem repeat1nstd128human GRCh37 chr16: 30,797,058-30,797,072 , GRCh38.p12 chr16: 30,785,737-30,785,751 ZNF629, RNF40
    nsv905732copy number variation1nstd71human NCBI36 chr16: 30,695,683-30,744,711 , GRCh37.p13 chr16: 30,788,182-30,837,210 , GRCh38.p12 chr16: 30,776,861-30,825,889 ZNF629, LOC647086, 1 more genes
    nsv6995541copy number variation1nstd229human GRCh38 chr16: 30,769,801-30,859,400 , GRCh37.p13 chr16: 30,781,122-30,870,721 ZNF629, BCL7C, 2 more genes
    nsv6505690copy number variation1nstd223human GRCh38 chr16: 30,780,611-30,867,997 , GRCh37.p13 chr16: 30,791,932-30,879,318 ZNF629, BCL7C, 2 more genes
    nsv4994624copy number variation1nstd200human GRCh38 chr16: 30,780,611-30,867,997 , GRCh37.p13 chr16: 30,791,932-30,879,318 ZNF629, BCL7C, 2 more genes
    nsv4245081copy number variation1nstd166human GRCh37.p13 chr16: 30,791,932-30,879,318 , GRCh38.p12 chr16: 30,780,611-30,867,997 ZNF629, BCL7C, 2 more genes
    nsv9438copy number variation1nstd4human NCBI35 chr16: 30,677,704-30,706,943 , GRCh37.p13 chr16: 30,770,203-30,799,442 , GRCh38.p12 chr16: 30,758,882-30,788,121 ZNF629, PHKG2, 2 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 ZNF629, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 ZNF629, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 ZNF629, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 ZNF629, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 ZNF629, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 ZNF629, LOC105371069, 654 more genes
    nsv3913895copy number variation1nstd102humanPathogenic NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592 ZNF629, ITGAL, 310 more genes
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