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Items: 1 to 20 of 136

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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
    nsv6977003copy number variation1nstd229human GRCh38 chr14: 100,933,679-100,938,887 , GRCh37.p13 chr14: 101,400,016-101,405,224 SNORD113-4, MEG8, 2 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
    nsv6510590copy number variation1nstd223human GRCh38 chr14: 100,939,775-100,940,248 , GRCh37.p13 chr14: 101,406,112-101,406,585 SNORD113-6, MEG8, 1 more genes
    nsv6498930copy number variation1nstd223human GRCh38 chr14: 100,938,245-100,938,767 , GRCh37.p13 chr14: 101,404,582-101,405,104 SNORD113-6, SNORD113-5, 1 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
    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
    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
    nsv3964607insertion1nstd168human GRCh38 chr14: 100,937,690-100,978,906 , GRCh37.p13 chr14: 101,404,027-101,445,243 SNORD113-7, SNORD114-1, 23 more genes
    nsv3924299copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,260,674-101,410,904 , GRCh38 chr14: 99,794,337-100,944,567 , NCBI36 chr14: 99,330,427-100,480,657 MIR433, RN7SKP92, 48 more genes
    nsv3922827copy number variation1nstd102humanPathogenic GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523 RNU6-1316P, MIR136, 440 more genes
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