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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672467insertion1nstd207human GRCh38 chr22: 32,147,902-32,147,902 , GRCh37.p13 chr22: 32,543,889-32,543,889 C22orf42
    nsv5665767insertion1nstd207human GRCh38 chr22: 32,151,064-32,151,064 , GRCh37.p13 chr22: 32,547,051-32,547,051 C22orf42
    nsv5601426copy number variation1nstd207human GRCh38 chr22: 32,149,798-32,151,041 , GRCh37.p13 chr22: 32,545,785-32,547,028 C22orf42
    nsv5587546copy number variation1nstd207human GRCh38 chr22: 32,141,886-32,148,340 , GRCh37.p13 chr22: 32,537,873-32,544,327 C22orf42
    nsv5552172copy number variation1nstd206human GRCh38 chr22: 32,130,274-32,170,624 , GRCh37.p13 chr22: 32,526,261-32,566,611 AP1B1P2, AP1B1P1, 1 more genes
    nsv5542773copy number variation1nstd206human GRCh38 chr22: 31,969,896-32,152,513 , GRCh37.p13 chr22: 32,365,883-32,548,500 SLC5A1, AP1B1P2, 6 more genes
    nsv5297264copy number variation1nstd204human GRCh38.p13 chr22: 32,144,601-32,150,400 , GRCh37.p13 chr22: 32,540,588-32,546,387 C22orf42
    nsv5178417mobile element insertion1nstd203human GRCh38 chr22: 32,150,904-32,150,920 , GRCh37.p13 chr22: 32,546,891-32,546,907 C22orf42
    nsv5167943mobile element insertion1nstd203human GRCh38 chr22: 32,160,327-32,160,341 , GRCh37.p13 chr22: 32,556,314-32,556,328 C22orf42
    nsv5161064mobile element insertion1nstd203human GRCh38 chr22: 32,150,001-32,150,011 , GRCh37.p13 chr22: 32,545,988-32,545,998 C22orf42
    nsv5039809copy number variation1nstd200human GRCh38 chr22: 31,969,895-32,152,514 , GRCh37.p13 chr22: 32,365,882-32,548,501 RPS17P16, SLC5A1, 6 more genes
    nsv5037691copy number variation1nstd200human GRCh38 chr22: 32,150,355-32,152,829 , GRCh37.p13 chr22: 32,546,342-32,548,816 C22orf42
    nsv5034652copy number variation1nstd200human GRCh38 chr22: 32,132,680-32,307,112 , GRCh37.p13 chr22: 32,528,667-32,703,099 RFPL2, AP1B1P2, 5 more genes
    nsv5031724copy number variation1nstd200human GRCh38 chr22: 32,130,274-32,170,624 , GRCh37.p13 chr22: 32,526,261-32,566,611 AP1B1P1, C22orf42, 1 more genes
    nsv5031295copy number variation1nstd200human GRCh38 chr22: 32,158,061-32,159,752 , GRCh37.p13 chr22: 32,554,048-32,555,739 C22orf42
    nsv5029866copy number variation1nstd200human GRCh38 chr22: 32,158,101-32,159,730 , GRCh37.p13 chr22: 32,554,088-32,555,717 C22orf42
    nsv5029423copy number variation1nstd200human GRCh38 chr22: 32,150,877-32,151,926 , GRCh37.p13 chr22: 32,546,864-32,547,913 C22orf42
    nsv4880038copy number variation1nstd200human GRCh37 chr22: 32,526,260-32,566,612 , GRCh38.p12 chr22: 32,130,273-32,170,625 C22orf42, AP1B1P2, 1 more genes
    nsv4872218copy number variation1nstd200human GRCh37 chr22: 32,554,048-32,555,739 , GRCh38.p12 chr22: 32,158,061-32,159,752 C22orf42
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
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