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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 more genes
    nsv6990401copy number variation1nstd229human GRCh38 chr17: 43,032,538-43,037,625 , GRCh37.p13 chr17: 41,184,555-41,189,642 RND2
    nsv6986012copy number variation1nstd229human GRCh38 chr17: 43,030,278-43,031,253 , GRCh37.p13 chr17: 41,182,295-41,183,270 RND2
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6637874copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,105,913-41,307,101 , GRCh38.p12 chr17: 42,953,896-43,155,084 RPL27, IFI35, 11 more genes
    nsv6191926copy number variation1nstd214human GRCh38 chr17: 43,025,660-43,025,724 , GRCh37.p13 chr17: 41,177,677-41,177,741 RND2
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 more genes
    nsv6088223insertion1nstd212human GRCh38 chr17: 43,024,257-43,024,257 , GRCh37.p13 chr17: 41,176,274-41,176,274 RND2
    nsv6027462copy number variation1nstd212human GRCh38 chr17: 43,024,227-43,024,329 , GRCh37.p13 chr17: 41,176,244-41,176,346 RND2
    nsv6023220copy number variation1nstd212human GRCh38 chr17: 43,024,258-43,024,446 , GRCh37.p13 chr17: 41,176,275-41,176,463 RND2
    nsv5651806insertion1nstd207human GRCh38 chr17: 43,024,257-43,024,257 , GRCh37.p13 chr17: 41,176,274-41,176,274 RND2
    nsv5557332sequence alteration1nstd206human GRCh38 chr17: 43,031,256-43,031,264 , GRCh37.p13 chr17: 41,183,273-41,183,281 RND2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5547390insertion1nstd206human GRCh38 chr17: 43,031,256-43,031,256 , GRCh37.p13 chr17: 41,183,273-41,183,273 RND2
    nsv5519425copy number variation1nstd206human GRCh38 chr17: 43,032,434-43,033,141 , GRCh37.p13 chr17: 41,184,451-41,185,158 RND2
    nsv5322811copy number variation1nstd204human GRCh38.p13 chr17: 43,032,408-43,033,170 , GRCh37.p13 chr17: 41,184,425-41,185,187 RND2
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5200268copy number variation1nstd205human GRCh37.p13 chr17: 41,184,364-41,222,054 , GRCh38.p12 chr17: 43,032,347-43,070,037 BRCA1, RND2
    nsv5159770mobile element insertion1nstd203human GRCh38 chr17: 43,024,304-43,024,330 , GRCh37.p13 chr17: 41,176,321-41,176,347 RND2
    nsv5159463mobile element insertion1nstd203human GRCh38 chr17: 43,024,241-43,024,257 , GRCh37.p13 chr17: 41,176,258-41,176,274 RND2
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