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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094497copy number variation2nstd102humanUncertain significance GRCh37 chr14: 35,182,071-35,873,850 , GRCh38.p12 chr14: 34,712,865-35,404,644 NFKBIA, IGBP1P1, 19 more genes
    nsv7093397copy number variation1nstd102humanPathogenic GRCh37 chr14: 34,904,407-36,784,136 , GRCh38.p12 chr14: 34,435,201-36,314,930 DPRXP3, LOC107984628, 51 more genes
    nsv7072225inversion1nstd229human GRCh38 chr14: 31,291,623-36,485,208 , GRCh37.p13 chr14: 31,760,829-36,954,413 LOC101927178, RNU7-93P, 84 more genes
    nsv7068116inversion1nstd229human GRCh38 chr14: 35,388,833-35,488,189 , GRCh37.p13 chr14: 35,858,039-35,957,395 NFKBIA, DNAJC8P1, 4 more genes
    nsv6577923inversion1nstd223human GRCh38 chr14: 35,388,831-35,488,187 , GRCh37.p13 chr14: 35,858,037-35,957,393 NFKBIA, RPLP0P3, 4 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6133124copy number variation1nstd213human GRCh37 chr14: 34,870,000-36,100,001 , GRCh38.p12 chr14: 34,400,794-35,630,795 SRP54, PRORP, 40 more genes
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4680263copy number variation1nstd189human GRCh37.p13 chr14: 34,948,278-35,870,835 , GRCh38.p12 chr14: 34,479,072-35,401,629 CFL2, NFKBIA, 31 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4624761copy number variation1nstd183human GRCh37 chr14: 35,864,558-35,874,170 , GRCh38.p12 chr14: 35,395,352-35,404,964 NFKBIA
    nsv4623518copy number variation1nstd183human GRCh37 chr14: 35,871,026-35,874,042 , GRCh38.p12 chr14: 35,401,820-35,404,836 NFKBIA
    nsv4620040copy number variation1nstd183human GRCh37 chr14: 35,872,066-35,872,240 , GRCh38.p12 chr14: 35,402,860-35,403,034 NFKBIA
    nsv4578383copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 35,873,764-35,873,899 , GRCh38 chr14: 35,404,558-35,404,693 NFKBIA
    nsv4573068sequence alteration1nstd166human GRCh38.p12 chr14: 35,388,831-35,488,264 , GRCh37.p13 chr14: 35,858,037-35,957,470 NFKBIA, RPLP0P3, 4 more genes
    nsv4228581copy number variation1nstd166human GRCh37.p13 chr14: 35,868,000-35,878,000 , GRCh38.p12 chr14: 35,398,794-35,408,794 NFKBIA
    nsv4227535copy number variation1nstd166human GRCh37.p13 chr14: 35,871,000-35,876,000 , GRCh38.p12 chr14: 35,401,794-35,406,794 NFKBIA
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