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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967009insertion1nstd209human GRCh38 chr9: 107,305,944-107,305,944 , GRCh37.p13 chr9: 110,068,225-110,068,225 RAD23B
    nsv5923331copy number variation1nstd209human GRCh38 chr9: 107,293,084-107,293,133 , GRCh37.p13 chr9: 110,055,365-110,055,414 RAD23B
    nsv5918084copy number variation1nstd209human GRCh38 chr9: 107,286,180-107,290,132 , GRCh37.p13 chr9: 110,048,461-110,052,413 RAD23B
    nsv5851176copy number variation1nstd209human GRCh38 chr9: 107,286,879-107,290,178 , GRCh37.p13 chr9: 110,049,160-110,052,459 RAD23B
    nsv5708430mobile element insertion2nstd211human GRCh38 chr9: 107,299,652-107,299,652 , GRCh37.p13 chr9: 110,061,933-110,061,933 RAD23B
    nsv5492876copy number variation1nstd206human GRCh38 chr9: 107,284,387-107,291,234 , GRCh37.p13 chr9: 110,046,668-110,053,515 RAD23B
    nsv5478525copy number variation1nstd206human GRCh38 chr9: 107,318,967-107,321,727 , GRCh37.p13 chr9: 110,081,248-110,084,008 RAD23B
    nsv5410540mobile element insertion1nstd206human GRCh38 chr9: 107,299,652-107,299,703 , GRCh37.p13 chr9: 110,061,933-110,061,984 RAD23B
    nsv5193182mobile element insertion1nstd203human GRCh38 chr9: 107,285,955-107,285,970 , GRCh37.p13 chr9: 110,048,236-110,048,251 RAD23B
    nsv5136228mobile element insertion1nstd203human GRCh38 chr9: 107,299,639-107,299,652 , GRCh37.p13 chr9: 110,061,920-110,061,933 RAD23B
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983043copy number variation1nstd200human GRCh38 chr9: 107,297,148-107,298,583 , GRCh37.p13 chr9: 110,059,429-110,060,864 RAD23B
    nsv4983042copy number variation1nstd200human GRCh38 chr9: 107,284,387-107,291,234 , GRCh37.p13 chr9: 110,046,668-110,053,515 RAD23B
    nsv4974803copy number variation1nstd200human GRCh38 chr9: 107,285,480-107,285,687 , GRCh37.p13 chr9: 110,047,761-110,047,968 RAD23B
    nsv4841005copy number variation1nstd200human GRCh37 chr9: 110,059,428-110,060,864 , GRCh38.p12 chr9: 107,297,147-107,298,583 RAD23B
    nsv4740584copy number variation1nstd199human GRCh37 chr9: 110,051,298-110,051,351 , GRCh38.p12 chr9: 107,289,017-107,289,070 RAD23B
    nsv4734985copy number variation1nstd199human GRCh37 chr9: 110,088,567-110,088,708 , GRCh38.p12 chr9: 107,326,286-107,326,427 RAD23B
    nsv4599161copy number variation1nstd183human GRCh37 chr9: 110,046,538-110,053,400 , GRCh38.p12 chr9: 107,284,257-107,291,119 RAD23B
    nsv4495766mobile element insertion1nstd166human GRCh37.p13 chr9: 110,061,920-110,061,920 , GRCh38.p12 chr9: 107,299,639-107,299,639 RAD23B
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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