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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115564mobile element insertion1nstd186human GRCh37 chr22: 42,633,105-42,633,156 , GRCh38.p12 chr22: 42,237,099-42,237,150 TCF20
    nsv5969380insertion1nstd209human GRCh38 chr22: 42,229,088-42,229,088 , GRCh37.p13 chr22: 42,625,094-42,625,094 TCF20
    nsv5967632insertion1nstd209human GRCh38 chr22: 42,242,227-42,242,227 , GRCh37.p13 chr22: 42,638,233-42,638,233 TCF20
    nsv5965961copy number variation1nstd209human GRCh38 chr22: 42,182,130-42,191,099 , GRCh37.p13 chr22: 42,578,136-42,587,105 TCF20
    nsv5963780copy number variation1nstd209human GRCh38 chr22: 42,224,236-42,232,591 , GRCh37.p13 chr22: 42,620,242-42,628,597 TCF20
    nsv5952866copy number variation1nstd209human GRCh38 chr22: 42,239,204-42,239,514 , GRCh37.p13 chr22: 42,635,210-42,635,520 TCF20
    nsv5879648copy number variation1nstd209human GRCh38 chr22: 42,182,134-42,191,087 , GRCh37.p13 chr22: 42,578,140-42,587,093 TCF20
    nsv5869732copy number variation1nstd209human GRCh38 chr22: 42,224,657-42,232,672 , GRCh37.p13 chr22: 42,620,663-42,628,678 TCF20
    nsv5707478mobile element insertion2nstd211human GRCh38 chr22: 42,229,097-42,229,097 , GRCh37.p13 chr22: 42,625,103-42,625,103 TCF20
    nsv5706668mobile element insertion2nstd211human GRCh38 chr22: 42,224,561-42,224,561 , GRCh37.p13 chr22: 42,620,567-42,620,567 TCF20
    nsv5699579mobile element insertion2nstd211human GRCh38 chr22: 42,237,099-42,237,099 , GRCh37.p13 chr22: 42,633,105-42,633,105 TCF20
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
    nsv5671450insertion1nstd207human GRCh38 chr22: 42,237,088-42,237,088 , GRCh37.p13 chr22: 42,633,094-42,633,094 TCF20
    nsv5665695insertion1nstd207human GRCh38 chr22: 42,166,381-42,166,381 , GRCh37.p13 chr22: 42,562,387-42,562,387 TCF20
    nsv5550921copy number variation1nstd206human GRCh38 chr22: 42,272,012-42,279,289 , GRCh37.p13 chr22: 42,668,018-42,675,295 OGFRP1, TCF20
    nsv5548721copy number variation1nstd206human GRCh38 chr22: 42,246,766-42,250,356 , GRCh37.p13 chr22: 42,642,772-42,646,362 TCF20
    nsv5547184copy number variation1nstd206human GRCh38 chr22: 42,222,330-42,223,502 , GRCh37.p13 chr22: 42,618,336-42,619,508 TCF20
    nsv5543896insertion1nstd206human GRCh38 chr22: 42,237,097-42,237,139 , GRCh37.p13 chr22: 42,633,103-42,633,145 TCF20
    nsv5540721copy number variation1nstd206human GRCh38 chr22: 42,239,180-42,245,928 , GRCh37.p13 chr22: 42,635,186-42,641,934 TCF20
    nsv5425138mobile element insertion1nstd206human GRCh38 chr22: 42,237,099-42,237,150 , GRCh37.p13 chr22: 42,633,105-42,633,156 TCF20
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