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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5931683copy number variation1nstd209human GRCh38 chr14: 81,528,774-81,529,859 , GRCh37.p13 chr14: 81,995,118-81,996,203 SEL1L
    nsv5857076copy number variation1nstd209human GRCh38 chr14: 81,528,769-81,529,768 , GRCh37.p13 chr14: 81,995,113-81,996,112 SEL1L
    nsv5705669mobile element insertion2nstd211human GRCh38 chr14: 81,491,944-81,491,944 , GRCh37.p13 chr14: 81,958,288-81,958,288 SEL1L
    nsv5702732mobile element insertion1nstd211human GRCh38 chr14: 81,473,182-81,473,182 , GRCh37.p13 chr14: 81,939,526-81,939,526 SEL1L
    nsv5701356mobile element insertion1nstd211human GRCh38 chr14: 81,514,468-81,514,468 , GRCh37.p13 chr14: 81,980,812-81,980,812 SEL1L
    nsv5660841insertion1nstd207human GRCh38 chr14: 81,491,929-81,491,929 , GRCh37.p13 chr14: 81,958,273-81,958,273 SEL1L
    nsv5647438insertion1nstd207human GRCh38 chr14: 81,492,781-81,492,781 , GRCh37.p13 chr14: 81,959,125-81,959,125 SEL1L
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5494098copy number variation1nstd206human GRCh38 chr14: 81,529,787-81,529,884 , GRCh37.p13 chr14: 81,996,131-81,996,228 SEL1L
    nsv5421166mobile element insertion1nstd206human GRCh38 chr14: 81,491,944-81,491,995 , GRCh37.p13 chr14: 81,958,288-81,958,339 SEL1L
    nsv5418871mobile element insertion1nstd206human GRCh38 chr14: 81,514,468-81,514,499 , GRCh37.p13 chr14: 81,980,812-81,980,843 SEL1L
    nsv5417173mobile element insertion1nstd206human GRCh38 chr14: 81,473,182-81,473,233 , GRCh37.p13 chr14: 81,939,526-81,939,577 SEL1L
    nsv5158085mobile element insertion1nstd203human GRCh38 chr14: 81,487,630-81,487,640 , GRCh37.p13 chr14: 81,953,974-81,953,984 SEL1L
    nsv5153926mobile element insertion1nstd203human GRCh38 chr14: 81,491,929-81,491,944 , GRCh37.p13 chr14: 81,958,273-81,958,288 SEL1L
    nsv5150887mobile element insertion1nstd203human GRCh38 chr14: 81,473,166-81,473,178 , GRCh37.p13 chr14: 81,939,510-81,939,522 SEL1L
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4501538mobile element insertion1nstd166human GRCh37.p13 chr14: 81,980,797-81,980,797 , GRCh38.p12 chr14: 81,514,453-81,514,453 SEL1L
    nsv4499480mobile element insertion1nstd166human GRCh37.p13 chr14: 81,958,273-81,958,273 , GRCh38.p12 chr14: 81,491,929-81,491,929 SEL1L
    nsv4456664copy number variation1nstd102humanPathogenic GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793 DYNLL1P2, GTF2A1, 126 more genes
    nsv4226317copy number variation1nstd166human GRCh37.p13 chr14: 81,929,092-82,046,685 , GRCh38.p12 chr14: 81,462,748-81,580,341 SEL1L
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