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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131381insertion1nstd186human GRCh37 chr15: 51,978,919-51,978,919 , GRCh38.p12 chr15: 51,686,722-51,686,722 SCG3
    nsv5977591inversion1nstd209human GRCh38 chr15: 51,686,722-51,694,466 , GRCh37.p13 chr15: 51,978,919-51,986,663 SCG3
    nsv5970075insertion1nstd209human GRCh38 chr15: 51,698,793-51,698,793 , GRCh37.p13 chr15: 51,990,990-51,990,990 SCG3
    nsv5936409copy number variation1nstd209human GRCh38 chr15: 51,691,911-51,691,964 , GRCh37.p13 chr15: 51,984,108-51,984,161 SCG3
    nsv5934490copy number variation1nstd209human GRCh38 chr15: 51,697,177-51,697,289 , GRCh37.p13 chr15: 51,989,374-51,989,486 SCG3
    nsv5713081mobile element insertion2nstd211human GRCh38 chr15: 51,689,165-51,689,165 , GRCh37.p13 chr15: 51,981,362-51,981,362 SCG3
    nsv5709037mobile element insertion2nstd211human GRCh38 chr15: 51,698,809-51,698,809 , GRCh37.p13 chr15: 51,991,006-51,991,006 SCG3
    nsv5649546insertion1nstd207human GRCh38 chr15: 51,698,793-51,698,793 , GRCh37.p13 chr15: 51,990,990-51,990,990 SCG3
    nsv5646999insertion1nstd207human GRCh38 chr15: 51,686,722-51,686,722 , GRCh37.p13 chr15: 51,978,919-51,978,919 SCG3
    nsv5593415copy number variation1nstd207human GRCh38 chr15: 51,691,911-51,691,964 , GRCh37.p13 chr15: 51,984,108-51,984,161 SCG3
    nsv5591301copy number variation1nstd207human GRCh38 chr15: 51,697,177-51,697,289 , GRCh37.p13 chr15: 51,989,374-51,989,486 SCG3
    nsv5548580insertion1nstd206human GRCh38 chr15: 51,704,274-51,704,295 , GRCh37.p13 chr15: 51,996,471-51,996,492 SCG3
    nsv5536924insertion1nstd206human GRCh38 chr15: 51,686,722-51,686,722 , GRCh37.p13 chr15: 51,978,919-51,978,919 SCG3
    nsv5517041copy number variation1nstd206human GRCh38 chr15: 51,697,179-51,697,290 , GRCh37.p13 chr15: 51,989,376-51,989,487 SCG3
    nsv5430666mobile element insertion1nstd206human GRCh38 chr15: 51,698,809-51,698,860 , GRCh37.p13 chr15: 51,991,006-51,991,057 SCG3
    nsv5420795mobile element insertion1nstd206human GRCh38 chr15: 51,689,165-51,689,216 , GRCh37.p13 chr15: 51,981,362-51,981,413 SCG3
    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
    nsv5301593copy number variation1nstd204human GRCh38.p13 chr15: 51,697,169-51,697,294 , GRCh37.p13 chr15: 51,989,366-51,989,491 SCG3
    nsv5154063mobile element insertion1nstd203human GRCh38 chr15: 51,689,257-51,689,264 , GRCh37.p13 chr15: 51,981,454-51,981,461 SCG3
    nsv5154030mobile element insertion1nstd203human GRCh38 chr15: 51,698,793-51,698,809 , GRCh37.p13 chr15: 51,990,990-51,991,006 SCG3
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