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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6970821copy number variation1nstd229human GRCh38 chr14: 101,391,345-101,625,639 , GRCh37.p13 chr14: 101,857,682-102,091,976 LINC00524, DIO3, 7 more genes
    nsv6967249copy number variation1nstd229human GRCh38 chr14: 101,560,058-101,560,459 , GRCh37.p13 chr14: 102,026,395-102,026,796 MIR1247, DIO3OS, 1 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
    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
    nsv6314048copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229 IGHD4-23, XRCC3, 329 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
    nsv6291499copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042 CDC42BPB, COA8, 133 more genes
    nsv6132860copy number variation1nstd213human GRCh37 chr14: 101,940,000-102,410,001 , GRCh38.p12 chr14: 101,473,663-101,943,664 RPL26P4, DIO3, 12 more genes
    nsv5511362copy number variation1nstd206human GRCh38 chr14: 101,556,234-101,557,963 , GRCh37.p13 chr14: 102,022,571-102,024,300 DIO3OS
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5311117copy number variation1nstd204human GRCh38.p13 chr14: 101,556,212-101,557,983 , GRCh37.p13 chr14: 102,022,549-102,024,320 DIO3OS
    nsv5276545copy number variation1nstd204human GRCh38.p13 chr14: 101,556,212-101,557,945 , GRCh37.p13 chr14: 102,022,549-102,024,282 DIO3OS
    nsv5265153copy number variation1nstd204human GRCh38.p13 chr14: 101,560,142-101,562,162 , GRCh37.p13 chr14: 102,026,479-102,028,499 MIR1247, DIO3OS, 1 more genes
    nsv5261446copy number variation1nstd204human GRCh38.p13 chr14: 101,556,201-101,557,900 , GRCh37.p13 chr14: 102,022,538-102,024,237 DIO3OS
    nsv4991415copy number variation1nstd200human GRCh38 chr14: 101,556,234-101,557,963 , GRCh37.p13 chr14: 102,022,571-102,024,300 DIO3OS
    nsv4854997copy number variation1nstd200human GRCh37 chr14: 102,022,571-102,024,300 , GRCh38.p12 chr14: 101,556,234-101,557,963 DIO3OS
    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
    nsv4621867copy number variation1nstd183human GRCh37 chr14: 102,026,707-102,027,542 , GRCh38.p12 chr14: 101,560,370-101,561,205 MIR1247, DIO3, 1 more genes
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 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
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