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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945659copy number variation1nstd209human GRCh38 chr16: 83,953,703-83,953,782 , GRCh37.p13 chr16: 83,987,308-83,987,387 OSGIN1
    nsv5662680insertion1nstd207human GRCh38 chr16: 83,951,962-83,951,962 , GRCh37.p13 chr16: 83,985,567-83,985,567 OSGIN1
    nsv5649943insertion1nstd207human GRCh38 chr16: 83,951,890-83,951,890 , GRCh37.p13 chr16: 83,985,495-83,985,495 , OSGIN1
    nsv5527976copy number variation1nstd206human GRCh38 chr16: 83,951,843-83,954,622 , GRCh37.p13 chr16: 83,985,448-83,988,227 , OSGIN1
    nsv5526880copy number variation1nstd206human GRCh38 chr16: 83,956,448-84,018,129 , GRCh37.p13 chr16: 83,990,053-84,051,734 SLC38A8, OSGIN1, 1 more genes
    nsv5358453translocation1nstd200human GRCh38 chr16: 83,965,430-83,965,430 , GRCh38 chr16: 83,965,333-83,965,333 , GRCh37.p13 chr16: 83,998,938-83,998,938 , GRCh37.p13 chr16: 83,999,035-83,999,035 OSGIN1
    nsv5358452translocation1nstd200human GRCh38 chr16: 83,953,705-83,953,705 , GRCh38 chr16: 83,953,783-83,953,783 , GRCh37.p13 chr16: 83,987,388-83,987,388 , GRCh37.p13 chr16: 83,987,310-83,987,310 OSGIN1
    nsv5308031copy number variation1nstd204human GRCh38.p13 chr16: 83,949,900-83,951,402 , GRCh37.p13 chr16: 83,983,505-83,985,007 , OSGIN1
    nsv5009829copy number variation1nstd200human GRCh38 chr16: 83,963,331-83,965,649 , GRCh37.p13 chr16: 83,996,936-83,999,254 OSGIN1
    nsv5009828copy number variation1nstd200human GRCh38 chr16: 83,961,721-84,055,568 , GRCh37.p13 chr16: 83,995,326-84,089,173 OSGIN1, MBTPS1, 3 more genes
    nsv5009821copy number variation1nstd200human GRCh38 chr16: 83,870,238-84,028,738 , GRCh37.p13 chr16: 83,903,843-84,062,343 , MLYCD, 4 more genes
    nsv4866985copy number variation1nstd200human GRCh37 chr16: 83,987,310-83,987,388 , GRCh38.p12 chr16: 83,953,705-83,953,783 OSGIN1
    nsv4755973insertion1nstd199human GRCh37 chr16: 83,985,327-83,985,327 , GRCh38.p12 chr16: 83,951,722-83,951,722 , OSGIN1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729844copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,866,931-85,276,940 , GRCh38.p12 chr16: 83,833,326-85,243,334 LOC105371376, MLYCD, 34 more genes
    nsv4685927copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 83,931,797-86,285,776 , GRCh38.p12 chr16: 83,898,192-86,252,170 COX4I1, IRF8, 57 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4680391copy number variation1nstd189human GRCh37.p13 chr16: 83,858,832-84,185,650 , GRCh38.p12 chr16: 83,825,227-84,152,045 , MBTPS1, 9 more genes
    nsv4680343copy number variation1nstd189human GRCh37.p13 chr16: 83,860,932-84,181,799 , GRCh38.p12 chr16: 83,827,327-84,148,194 , MBTPS1, 9 more genes
    nsv4675771copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,853,228-84,189,313 , GRCh38.p12 chr16: 83,819,623-84,155,708 DNAAF1, LOC648774, 9 more genes
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