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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094272copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,080,779-97,347,545 , GRCh38.p12 chr14: 94,614,442-96,881,208 ADIPOR1P2, LOC105370637, 48 more genes
    nsv7059017inversion1nstd229human GRCh38 chr14: 96,226,465-96,562,101 , GRCh37.p13 chr14: 96,692,802-97,028,438 PAPOLA-DT, BDKRB1, 8 more genes
    nsv6974489copy number variation1nstd229human GRCh38 chr14: 96,364,901-96,366,300 , GRCh37.p13 chr14: 96,831,238-96,832,637 GSKIP
    nsv6973725copy number variation1nstd229human GRCh38 chr14: 96,364,935-96,366,352 , GRCh37.p13 chr14: 96,831,272-96,832,689 GSKIP
    nsv6971756copy number variation1nstd229human GRCh38 chr14: 96,334,795-96,477,903 , GRCh37.p13 chr14: 96,801,132-96,944,240 AK7, GSKIP, 4 more genes
    nsv6969851copy number variation1nstd229human GRCh38 chr14: 96,365,625-96,366,210 , GRCh37.p13 chr14: 96,831,962-96,832,547 GSKIP
    nsv6963956copy number variation1nstd229human GRCh38 chr14: 96,323,375-96,463,489 , GRCh37.p13 chr14: 96,789,712-96,929,826 ATG2B, RPL23AP10, 4 more genes
    nsv6958962copy number variation1nstd229human GRCh38 chr14: 96,381,347-96,416,916 , GRCh37.p13 chr14: 96,847,684-96,883,253 AK7, GSKIP, 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
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6582121inversion1nstd223human GRCh38 chr14: 96,371,475-96,373,230 , GRCh37.p13 chr14: 96,837,812-96,839,567 GSKIP
    nsv6514163copy number variation1nstd223human GRCh38 chr14: 96,364,935-96,366,310 , GRCh37.p13 chr14: 96,831,272-96,832,647 GSKIP
    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
    nsv6132796copy number variation1nstd213human GRCh37 chr14: 96,660,000-97,840,001 , GRCh38.p12 chr14: 96,193,663-97,373,664 PAPOLA, ATG2B, 16 more genes
    nsv5944035copy number variation1nstd209human GRCh38 chr14: 96,364,894-96,366,309 , GRCh37.p13 chr14: 96,831,231-96,832,646 GSKIP
    nsv5856343copy number variation1nstd209human GRCh38 chr14: 96,364,903-96,366,302 , GRCh37.p13 chr14: 96,831,240-96,832,639 GSKIP
    nsv5602878copy number variation1nstd207human GRCh38 chr14: 96,364,894-96,366,309 , GRCh37.p13 chr14: 96,831,231-96,832,646 GSKIP
    nsv5507983copy number variation1nstd206human GRCh38 chr14: 96,364,909-96,366,334 , GRCh37.p13 chr14: 96,831,246-96,832,671 GSKIP
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