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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973562insertion1nstd209human GRCh38 chr15: 49,476,230-49,476,230 , GRCh37.p13 chr15: 49,768,427-49,768,427 FAM227B, FGF7
    nsv5933975copy number variation1nstd209human GRCh38 chr15: 49,430,331-49,430,471 , GRCh37.p13 chr15: 49,722,528-49,722,668 FGF7, FAM227B
    nsv5721955mobile element insertion1nstd211human GRCh38 chr15: 49,465,006-49,465,006 , GRCh37.p13 chr15: 49,757,203-49,757,203 FGF7, FAM227B
    nsv5715666mobile element insertion1nstd211human GRCh38 chr15: 49,457,982-49,457,982 , GRCh37.p13 chr15: 49,750,179-49,750,179 FAM227B, FGF7
    nsv5710940mobile element insertion1nstd211human GRCh38 chr15: 49,476,245-49,476,245 , GRCh37.p13 chr15: 49,768,442-49,768,442 FGF7, FAM227B
    nsv5652200insertion1nstd207human GRCh38 chr15: 49,471,232-49,471,232 , GRCh37.p13 chr15: 49,763,429-49,763,429 FAM227B, FGF7
    nsv5562138inversion1nstd206human GRCh38 chr15: 49,468,865-49,474,654 , GRCh37.p13 chr15: 49,761,062-49,766,851 FGF7, FAM227B
    nsv5554462mobile element insertion1nstd206human GRCh38 chr15: 49,465,006-49,465,057 , GRCh37.p13 chr15: 49,757,203-49,757,254 FAM227B, FGF7
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5270216copy number variation1nstd204human GRCh38.p13 chr15: 49,455,901-49,458,900 , GRCh37.p13 chr15: 49,748,098-49,751,097 FAM227B, FGF7
    nsv5264703copy number variation1nstd204human GRCh38.p13 chr15: 49,444,901-49,448,200 , GRCh37.p13 chr15: 49,737,098-49,740,397 FAM227B, FGF7
    nsv5155599mobile element insertion1nstd203human GRCh38 chr15: 49,476,224-49,476,232 , GRCh37.p13 chr15: 49,768,421-49,768,429 FAM227B, FGF7
    nsv5141891mobile element insertion1nstd203human GRCh38 chr15: 49,476,232-49,476,245 , GRCh37.p13 chr15: 49,768,429-49,768,442 FAM227B, FGF7
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5033879inversion1nstd200human GRCh38 chr15: 49,468,891-49,474,631 , GRCh37.p13 chr15: 49,761,088-49,766,828 FGF7, FAM227B
    nsv5005373copy number variation1nstd200human GRCh38 chr15: 49,470,728-49,471,018 , GRCh37.p13 chr15: 49,762,925-49,763,215 FGF7, FAM227B
    nsv5001719copy number variation1nstd200human GRCh38 chr15: 49,487,398-49,488,986 , GRCh37.p13 chr15: 49,779,595-49,781,183 FGF7, FAM227B, 1 more genes
    nsv4886779inversion1nstd200human GRCh37 chr15: 49,761,087-49,766,828 , GRCh38.p12 chr15: 49,468,890-49,474,631 FAM227B, FGF7
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866100copy number variation1nstd200human GRCh37 chr15: 49,760,457-49,760,834 , GRCh38.p12 chr15: 49,468,260-49,468,637 FAM227B, FGF7
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