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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130789insertion1nstd186human GRCh37 chr16: 19,517,515-19,517,562 , GRCh38.p12 chr16: 19,506,193-19,506,240 GDE1
    nsv5977898insertion1nstd209human GRCh38 chr16: 19,506,179-19,506,179 , GRCh37.p13 chr16: 19,517,501-19,517,501 GDE1
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5715716mobile element insertion2nstd211human GRCh38 chr16: 19,512,668-19,512,668 , GRCh37.p13 chr16: 19,523,990-19,523,990 GDE1
    nsv5711939mobile element insertion2nstd211human GRCh38 chr16: 19,500,691-19,500,691 , GRCh37.p13 chr16: 19,512,013-19,512,013 GDE1
    nsv5700955mobile element insertion2nstd211human GRCh38 chr16: 19,506,193-19,506,193 , GRCh37.p13 chr16: 19,517,515-19,517,515 GDE1
    nsv5696114mobile element insertion2nstd211human GRCh38 chr16: 19,512,333-19,512,333 , GRCh37.p13 chr16: 19,523,655-19,523,655 GDE1
    nsv5662106insertion1nstd207human GRCh38 chr16: 19,506,179-19,506,179 , GRCh37.p13 chr16: 19,517,501-19,517,501 GDE1
    nsv5652488insertion1nstd207human GRCh38 chr16: 19,500,680-19,500,680 , GRCh37.p13 chr16: 19,512,002-19,512,002 GDE1
    nsv5645829insertion1nstd207human GRCh38 chr16: 19,517,657-19,517,657 , GRCh37.p13 chr16: 19,528,979-19,528,979 GDE1
    nsv5542839insertion1nstd206human GRCh38 chr16: 19,506,193-19,506,240 , GRCh37.p13 chr16: 19,517,515-19,517,562 GDE1
    nsv5428563mobile element insertion1nstd206human GRCh38 chr16: 19,512,333-19,512,384 , GRCh37.p13 chr16: 19,523,655-19,523,706 GDE1
    nsv5415043mobile element insertion1nstd206human GRCh38 chr16: 19,500,691-19,500,742 , GRCh37.p13 chr16: 19,512,013-19,512,064 GDE1
    nsv5301429copy number variation1nstd204human GRCh37.p13 chr16: 19,504,897-19,512,920 , GRCh38.p13 chr16: 19,493,575-19,501,598 GDE1, TMC5, 1 more genes
    nsv5280082copy number variation1nstd204human GRCh38.p13 chr16: 19,493,571-19,500,046 , GRCh37.p13 chr16: 19,504,893-19,511,368 TMC5, RNU4-46P, 1 more genes
    nsv5271986copy number variation1nstd204human GRCh38.p13 chr16: 19,499,701-19,501,700 , GRCh37.p13 chr16: 19,511,023-19,513,022 GDE1
    nsv5264906copy number variation1nstd204human GRCh38.p13 chr16: 19,491,501-19,501,600 , GRCh37.p13 chr16: 19,502,823-19,512,922 TMC5, RNU4-46P, 1 more genes
    nsv5157627mobile element insertion1nstd203human GRCh38 chr16: 19,506,193-19,506,193 , GRCh37.p13 chr16: 19,517,515-19,517,515 GDE1
    nsv5156459mobile element insertion1nstd203human GRCh38 chr16: 19,500,680-19,500,691 , GRCh37.p13 chr16: 19,512,002-19,512,013 GDE1
    nsv5147874mobile element insertion1nstd203human GRCh38 chr16: 19,506,192-19,506,192 , GRCh37.p13 chr16: 19,517,514-19,517,514 GDE1
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