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Items: 1 to 20 of 394

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7093141copy number variation1nstd102humanUncertain significance GRCh37 chr20: 42,247,452-42,247,589 , GRCh38 chr20: 43,618,812-43,618,949 IFT52
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 more genes
    nsv7063922inversion1nstd229human GRCh38 chr20: 43,626,165-43,772,216 , GRCh37.p13 chr20: 42,254,805-42,400,856 RPL27AP, IFT52, 3 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7061700inversion1nstd229human GRCh38 chr20: 43,564,590-43,703,553 , GRCh37.p13 chr20: 42,193,230-42,332,193 SGK2, RPL27AP, 2 more genes
    nsv7036207copy number variation1nstd229human GRCh38 chr20: 43,620,131-43,623,402 , GRCh37.p13 chr20: 42,248,771-42,252,042 IFT52
    nsv7034109copy number variation1nstd229human GRCh38 chr20: 43,613,401-43,630,000 , GRCh37.p13 chr20: 42,242,041-42,258,640 IFT52
    nsv7032569copy number variation1nstd229human GRCh38 chr20: 43,631,036-43,692,886 , GRCh37.p13 chr20: 42,259,676-42,321,526 IFT52, RPL27AP, 1 more genes
    nsv7032488copy number variation1nstd229human GRCh38 chr20: 43,643,201-43,645,900 , GRCh37.p13 chr20: 42,271,841-42,274,540 IFT52
    nsv7024142copy number variation1nstd229human GRCh38 chr20: 43,604,157-43,604,552 , GRCh37.p13 chr20: 42,232,797-42,233,192 IFT52
    nsv7022544copy number variation1nstd229human GRCh38 chr20: 43,638,501-43,641,800 , GRCh37.p13 chr20: 42,267,141-42,270,440 IFT52
    nsv7021263copy number variation1nstd229human GRCh38 chr20: 43,590,311-43,770,924 , GRCh37.p13 chr20: 42,218,951-42,399,564 GTSF1L, MYBL2, 3 more genes
    nsv7019168copy number variation1nstd229human GRCh38 chr20: 43,628,585-43,631,702 , GRCh37.p13 chr20: 42,257,225-42,260,342 IFT52
    nsv7018113copy number variation1nstd229human GRCh38 chr20: 43,587,226-43,589,909 , GRCh37.p13 chr20: 42,215,866-42,218,549 IFT52
    nsv6626699copy number variation1nstd224human GRCh37 chr20: 42,232,903-42,328,424 , GRCh38.p12 chr20: 43,604,263-43,699,784 IFT52, MYBL2, 1 more genes
    nsv6599750inversion1nstd223human GRCh38 chr20: 43,632,272-43,633,339 , GRCh37.p13 chr20: 42,260,912-42,261,979 IFT52
    nsv6598007inversion1nstd223human GRCh38 chr20: 43,593,575-43,594,322 , GRCh37.p13 chr20: 42,222,215-42,222,962 IFT52
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6595900inversion1nstd223human GRCh38 chr20: 43,641,827-43,642,885 , GRCh37.p13 chr20: 42,270,467-42,271,525 IFT52
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