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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5659968insertion1nstd207human GRCh38 chr14: 101,038,305-101,038,305 , GRCh37.p13 chr14: 101,504,642-101,504,642 MIR376C, MIR376A2, 1 more genes
    nsv5659748insertion1nstd207human GRCh38 chr14: 101,038,614-101,038,614 , GRCh37.p13 chr14: 101,504,951-101,504,951 MIR376C, MIR376B, 2 more genes
    nsv5648097insertion1nstd207human GRCh38 chr14: 101,038,566-101,038,566 , GRCh37.p13 chr14: 101,504,903-101,504,903 MIR376C, MIR376B, 2 more genes
    nsv5645252insertion1nstd207human GRCh38 chr14: 101,038,311-101,038,311 , GRCh37.p13 chr14: 101,504,648-101,504,648 MIR376C, MIR376A2, 1 more genes
    nsv5603395copy number variation1nstd207human GRCh38 chr14: 101,038,225-101,038,298 , GRCh37.p13 chr14: 101,504,562-101,504,635 MIR376C, MIR376A2, 1 more genes
    nsv5602619copy number variation1nstd207human GRCh38 chr14: 101,038,356-101,038,529 , GRCh37.p13 chr14: 101,504,693-101,504,866 MIR376C, MIR376B, 2 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
    nsv4740436copy number variation1nstd199human GRCh38.p12 chr14: 101,038,177-101,038,243 , GRCh37 chr14: 101,504,514-101,504,580 MIR376C, MIR376A2, 1 more genes
    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
    nsv4645337copy number variation1nstd186human GRCh37 chr14: 101,461,351-101,532,406 , GRCh38.p12 chr14: 100,995,014-101,066,069 MIR381HG, MIR758, 42 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
    nsv4449324copy number variation1nstd175human GRCh38.p12 chr14: 101,038,180-101,038,315 , GRCh37 chr14: 101,504,517-101,504,652 MIR376C, MIR376A2, 1 more genes
    nsv4424384copy number variation1nstd174human GRCh37 chr14: 101,504,330-101,505,201 , GRCh38.p12 chr14: 101,037,993-101,038,864 MIR376C, MIR376A1, 3 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
    nsv4349480copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,575,917-107,281,934 , GRCh38.p12 chr14: 100,109,580-106,873,725 IGHD2-21, MIR300, 452 more genes
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