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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148136copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125 SNORD113-5, SNORD114-27, 99 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
    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
    nsv6086819insertion1nstd212human GRCh38 chr14: 100,873,455-100,873,455 , GRCh37.p13 chr14: 101,339,792-101,339,792 MIR337, MIR665
    nsv6029807copy number variation1nstd212human GRCh38 chr14: 100,873,202-100,873,475 , GRCh37.p13 chr14: 101,339,539-101,339,812 MIR337, MIR665
    nsv5972102insertion1nstd209human GRCh38 chr14: 100,873,455-100,873,455 , GRCh37.p13 chr14: 101,339,792-101,339,792 MIR337, MIR665
    nsv5650391insertion1nstd207human GRCh38 chr14: 100,873,455-100,873,455 , GRCh37.p13 chr14: 101,339,792-101,339,792 MIR337, MIR665
    nsv5543249insertion1nstd206human GRCh38 chr14: 100,873,255-100,873,320 , GRCh37.p13 chr14: 101,339,592-101,339,657 MIR665, MIR337
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5273866copy number variation1nstd204human GRCh38.p13 chr14: 100,869,962-100,872,536 , GRCh37.p13 chr14: 101,336,299-101,338,873 MIR337
    nsv5264787copy number variation1nstd204human GRCh38.p13 chr14: 100,871,701-100,873,200 , GRCh37.p13 chr14: 101,338,038-101,339,537 MIR337, MIR665
    nsv4730960copy number variation1nstd199human GRCh38.p12 chr14: 100,873,198-100,873,887 , GRCh37 chr14: 101,339,535-101,340,224 MIR337, MIR665
    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
    nsv4530017copy number variation1nstd166human GRCh37.p13 chr14: 101,339,662-101,339,792 , GRCh38.p12 chr14: 100,873,325-100,873,455 MIR665, MIR337
    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
    nsv4445737insertion1nstd175human GRCh37 chr14: 101,339,787-101,339,787 , GRCh38.p12 chr14: 100,873,450-100,873,450 MIR337, MIR665
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