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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6973705copy number variation1nstd229human GRCh38 chr14: 98,711,763-98,727,447 , GRCh37.p13 chr14: 99,178,100-99,193,784 LINC02914
    nsv6972661copy number variation1nstd229human GRCh38 chr14: 98,711,579-98,727,447 , GRCh37.p13 chr14: 99,177,916-99,193,784 LINC02914
    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
    nsv6970654copy number variation1nstd229human GRCh38 chr14: 98,697,781-98,712,032 , GRCh37.p13 chr14: 99,164,118-99,178,369 LINC02914
    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
    nsv6622934copy number variation1nstd224human GRCh37 chr14: 99,182,535-99,202,206 , GRCh38.p12 chr14: 98,716,198-98,735,869 LINC02914
    nsv6622933copy number variation37nstd224human GRCh37 chr14: 99,182,535-99,193,023 , GRCh38.p12 chr14: 98,716,198-98,726,686 LINC02914
    nsv6622762copy number variation1nstd224human GRCh37 chr14: 99,182,536-99,193,023 , GRCh38.p12 chr14: 98,716,199-98,726,686 LINC02914
    nsv6575593inversion1nstd223human GRCh38 chr14: 98,711,014-98,713,745 , GRCh37.p13 chr14: 99,177,351-99,180,082 LINC02914
    nsv6506274copy number variation1nstd223human GRCh38 chr14: 98,711,763-98,727,446 , GRCh37.p13 chr14: 99,178,100-99,193,783 LINC02914
    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
    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
    nsv6082845insertion1nstd212human GRCh38 chr14: 98,710,546-98,710,546 , GRCh37.p13 chr14: 99,176,883-99,176,883 LINC02914
    nsv5931533copy number variation1nstd209human GRCh38 chr14: 98,711,763-98,727,445 , GRCh37.p13 chr14: 99,178,100-99,193,782 LINC02914
    nsv5864514copy number variation1nstd209human GRCh38 chr14: 98,711,700-98,725,769 , GRCh37.p13 chr14: 99,178,037-99,192,106 LINC02914
    nsv5505851copy number variation1nstd206human GRCh38 chr14: 98,711,763-98,727,446 , GRCh37.p13 chr14: 99,178,100-99,193,783 LINC02914
    nsv5498773copy number variation1nstd206human GRCh38 chr14: 98,711,718-98,712,008 , GRCh37.p13 chr14: 99,178,055-99,178,345 LINC02914
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5330601translocation1nstd200human GRCh37 chr14: 99,178,100-99,178,100 , GRCh37 chr14: 99,193,783-99,193,783 , GRCh38.p12 chr14: 98,711,763-98,711,763 , GRCh38.p12 chr14: 98,727,446-98,727,446 LINC02914
    nsv5319762copy number variation1nstd204human GRCh38.p13 chr14: 98,711,736-98,727,468 , GRCh37.p13 chr14: 99,178,073-99,193,805 LINC02914
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