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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148098copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427 BCL7A, HPD, 14 more genes
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv6936710copy number variation1nstd229human GRCh38 chr12: 121,939,547-121,939,619 , GRCh37.p13 chr12: 122,377,453-122,377,525 CFAP251
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934155copy number variation1nstd229human GRCh38 chr12: 121,938,548-121,947,519 , GRCh37.p13 chr12: 122,376,454-122,385,425 CFAP251
    nsv6932296copy number variation1nstd229human GRCh38 chr12: 121,991,204-121,991,472 , GRCh37.p13 chr12: 122,429,110-122,429,378 CFAP251
    nsv6930497copy number variation1nstd229human GRCh38 chr12: 121,931,945-121,944,584 , GRCh37.p13 chr12: 122,369,851-122,382,490 CFAP251
    nsv6930271copy number variation1nstd229human GRCh38 chr12: 121,926,201-121,930,300 , GRCh37.p13 chr12: 122,364,107-122,368,206 CFAP251
    nsv6928899copy number variation1nstd229human GRCh38 chr12: 121,923,346-121,924,710 , GRCh37.p13 chr12: 122,361,252-122,362,616 CFAP251
    nsv6927967copy number variation1nstd229human GRCh38 chr12: 121,965,611-121,968,868 , GRCh37.p13 chr12: 122,403,517-122,406,774 CFAP251
    nsv6927878copy number variation1nstd229human GRCh38 chr12: 121,964,858-121,967,617 , GRCh37.p13 chr12: 122,402,764-122,405,523 CFAP251
    nsv6925490copy number variation1nstd229human GRCh38 chr12: 121,932,617-121,938,034 , GRCh37.p13 chr12: 122,370,523-122,375,940 CFAP251
    nsv6925455copy number variation1nstd229human GRCh38 chr12: 121,924,522-121,931,232 , GRCh37.p13 chr12: 122,362,428-122,369,138 CFAP251
    nsv6924253copy number variation1nstd229human GRCh38 chr12: 121,979,613-121,990,618 , GRCh37.p13 chr12: 122,417,519-122,428,524 CFAP251
    nsv6922344copy number variation1nstd229human GRCh38 chr12: 121,983,501-121,989,800 , GRCh37.p13 chr12: 122,421,407-122,427,706 CFAP251
    nsv6920920copy number variation1nstd229human GRCh38 chr12: 121,001,001-122,266,400 , GRCh37.p13 chr12: 121,438,804-122,750,947 BCL7A, KDM2B, 36 more genes
    nsv6920186copy number variation1nstd229human GRCh38 chr12: 121,951,007-121,959,912 , GRCh37.p13 chr12: 122,388,913-122,397,818 CFAP251
    nsv6919516copy number variation1nstd229human GRCh38 chr12: 121,977,648-121,977,948 , GRCh37.p13 chr12: 122,415,554-122,415,854 CFAP251
    nsv6919448copy number variation1nstd229human GRCh38 chr12: 121,987,815-121,990,760 , GRCh37.p13 chr12: 122,425,721-122,428,666 CFAP251
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