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Items: 1 to 20 of 422

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6972475copy number variation1nstd229human GRCh38 chr14: 99,175,901-99,949,300 , GRCh37.p13 chr14: 99,642,238-100,415,637 SETD3, LOC105370661, 10 more genes
    nsv6972243copy number variation1nstd229human GRCh38 chr14: 98,444,126-100,047,287 , GRCh37.p13 chr14: 98,910,463-100,513,624 CYP46A1, RPS2P3, 19 more genes
    nsv6972062copy number variation1nstd229human GRCh38 chr14: 99,157,768-99,175,311 , GRCh37.p13 chr14: 99,624,105-99,641,648 BCL11B
    nsv6971469copy number variation1nstd229human GRCh38 chr14: 99,242,368-99,245,350 , GRCh37.p13 chr14: 99,708,705-99,711,687 BCL11B
    nsv6969583copy number variation1nstd229human GRCh38 chr14: 99,223,561-99,223,592 , GRCh37.p13 chr14: 99,689,898-99,689,929 BCL11B
    nsv6968255copy number variation1nstd229human GRCh38 chr14: 99,175,601-99,684,700 , GRCh37.p13 chr14: 99,641,938-100,151,037 BCL11B, CCDC85C, 7 more genes
    nsv6962696copy number variation1nstd229human GRCh38 chr14: 99,175,301-99,270,900 , GRCh37.p13 chr14: 99,641,638-99,737,237 BCL11B
    nsv6962464copy number variation1nstd229human GRCh38 chr14: 99,249,807-99,253,661 , GRCh37.p13 chr14: 99,716,144-99,719,998 BCL11B
    nsv6961907copy number variation1nstd229human GRCh38 chr14: 99,211,654-99,226,232 , GRCh37.p13 chr14: 99,677,991-99,692,569 BCL11B
    nsv6961613copy number variation1nstd229human GRCh38 chr14: 99,269,701-99,272,800 , GRCh37.p13 chr14: 99,736,038-99,739,137 BCL11B
    nsv6960661copy number variation1nstd229human GRCh38 chr14: 99,185,470-99,185,778 , GRCh37.p13 chr14: 99,651,807-99,652,115 BCL11B
    nsv6959238copy number variation1nstd229human GRCh38 chr14: 99,250,892-99,253,997 , GRCh37.p13 chr14: 99,717,229-99,720,334 BCL11B
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6511162copy number variation1nstd223human GRCh38 chr14: 99,249,807-99,253,658 , GRCh37.p13 chr14: 99,716,144-99,719,995 BCL11B
    nsv6508607copy number variation1nstd223human GRCh38 chr14: 99,185,473-99,185,778 , GRCh37.p13 chr14: 99,651,810-99,652,115 BCL11B
    nsv6504885copy number variation1nstd223human GRCh38 chr14: 99,242,368-99,245,341 , GRCh37.p13 chr14: 99,708,705-99,711,678 BCL11B
    nsv6498487copy number variation1nstd223human GRCh38 chr14: 99,211,654-99,226,232 , GRCh37.p13 chr14: 99,677,991-99,692,569 BCL11B
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6309773copy number variation1nstd102humanUncertain significance GRCh37 chr14: 99,640,488-99,737,555 , GRCh38.p12 chr14: 99,174,151-99,271,218 BCL11B
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
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