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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6974484copy number variation1nstd229human GRCh38 chr14: 101,004,154-101,513,562 , GRCh37.p13 chr14: 101,470,491-101,979,899 MIR541, MIR487A, 49 more genes
    nsv6969834copy number variation1nstd229human GRCh38 chr14: 101,051,871-101,135,756 , GRCh37.p13 chr14: 101,518,208-101,602,093 MIR323B, MIR381HG, 17 more genes
    nsv6966086copy number variation1nstd229human GRCh38 chr14: 101,038,368-101,163,500 , GRCh37.p13 chr14: 101,504,705-101,629,837 MIR889, MIR382, 31 more genes
    nsv6958859copy number variation1nstd229human GRCh38 chr14: 100,868,127-101,331,726 , GRCh37.p13 chr14: 101,334,464-101,798,063 MIR136, MIR329-2, 97 more genes
    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
    nsv6622433copy number variation1nstd224human GRCh37 chr14: 101,470,596-101,943,950 , GRCh38.p12 chr14: 101,004,259-101,477,613 MIR154, MIR299, 49 more genes
    nsv6512298copy number variation1nstd223human GRCh38 chr14: 101,004,154-101,513,562 , GRCh37.p13 chr14: 101,470,491-101,979,899 MIR323B, MIR1193, 49 more genes
    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
    nsv6132885copy number variation1nstd213human GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664 DLK1, MEG8, 135 more genes
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5005000copy number variation1nstd200human GRCh38 chr14: 101,004,154-101,513,562 , GRCh37.p13 chr14: 101,470,491-101,979,899 , MIR655, 50 more genes
    nsv4991406copy number variation1nstd200human GRCh38 chr14: 101,068,062-101,068,208 , GRCh37.p13 chr14: 101,534,399-101,534,545 MEG9
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4618949copy number variation1nstd183human GRCh37 chr14: 101,372,908-101,884,282 , GRCh38.p12 chr14: 100,906,571-101,417,945 , LOC100128373, 90 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4413532copy number variation1nstd174human GRCh37 chr14: 101,372,741-101,967,655 , GRCh38.p12 chr14: 100,906,404-101,501,318 , MIR369, 92 more genes
    nsv4413343copy number variation1nstd174human GRCh37 chr14: 101,472,616-101,716,200 , GRCh38.p12 chr14: 101,006,279-101,249,863 MIR323A, MIR376C, 45 more genes
    nsv4349898copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 99,737,888-101,847,855 , GRCh38.p12 chr14: 99,271,551-101,381,518 EML1, WARS1, 136 more genes
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