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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5703136mobile element insertion2nstd211human GRCh38 chr14: 96,074,331-96,074,331 , GRCh37.p13 chr14: 96,540,668-96,540,668 C14orf132
    nsv5539413insertion1nstd206human GRCh38 chr14: 96,053,093-96,053,102 , GRCh37.p13 chr14: 96,519,430-96,519,439 C14orf132
    nsv5503254copy number variation1nstd206human GRCh38 chr14: 96,090,028-96,112,653 , GRCh37.p13 chr14: 96,556,365-96,578,990 C14orf132
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5496872copy number variation1nstd206human GRCh38 chr14: 96,061,029-96,069,361 , GRCh37.p13 chr14: 96,527,366-96,535,698 C14orf132
    nsv5418777mobile element insertion1nstd206human GRCh38 chr14: 96,074,331-96,074,382 , GRCh37.p13 chr14: 96,540,668-96,540,719 C14orf132
    nsv5357577translocation1nstd200human GRCh38 chr14: 96,072,450-96,072,450 , GRCh38 chr14: 96,072,354-96,072,354 , GRCh37.p13 chr14: 96,538,691-96,538,691 , GRCh37.p13 chr14: 96,538,787-96,538,787 C14orf132
    nsv5311796copy number variation1nstd204human GRCh38.p13 chr14: 96,056,297-96,070,077 , GRCh37.p13 chr14: 96,522,634-96,536,414 C14orf132
    nsv5304517copy number variation1nstd204human GRCh38.p13 chr14: 96,061,027-96,069,369 , GRCh37.p13 chr14: 96,527,364-96,535,706 C14orf132
    nsv5275165copy number variation1nstd204human GRCh38.p13 chr14: 96,061,101-96,069,300 , GRCh37.p13 chr14: 96,527,438-96,535,637 C14orf132
    nsv5271189copy number variation1nstd204human GRCh38.p13 chr14: 96,055,799-96,070,247 , GRCh37.p13 chr14: 96,522,136-96,536,584 C14orf132
    nsv5268413copy number variation1nstd204human GRCh38.p13 chr14: 96,060,649-96,069,222 , GRCh37.p13 chr14: 96,526,986-96,535,559 C14orf132
    nsv5155761mobile element insertion1nstd203human GRCh38 chr14: 96,074,321-96,074,331 , GRCh37.p13 chr14: 96,540,658-96,540,668 C14orf132
    nsv5007435copy number variation1nstd200human GRCh38 chr14: 96,061,029-96,069,361 , GRCh37.p13 chr14: 96,527,366-96,535,698 C14orf132
    nsv5004962copy number variation1nstd200human GRCh38 chr14: 96,056,300-96,070,075 , GRCh37.p13 chr14: 96,522,637-96,536,412 C14orf132
    nsv4849575copy number variation1nstd200human GRCh37 chr14: 96,527,366-96,535,698 , GRCh38.p12 chr14: 96,061,029-96,069,361 C14orf132
    nsv4734886copy number variation1nstd199human GRCh37 chr14: 96,515,818-96,515,890 , GRCh38.p12 chr14: 96,049,481-96,049,553 C14orf132
    nsv4675940copy number variation1nstd102humanUncertain significance GRCh37 chr14: 96,509,822-96,832,238 , GRCh38.p12 chr14: 96,043,485-96,365,901 CKS1BP1, BDKRB1, 4 more genes
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4674921copy number variation1nstd102humanLikely benign GRCh37 chr14: 96,453,503-96,589,931 , GRCh38.p12 chr14: 95,987,166-96,123,594 C14orf132
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