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Items: 1 to 20 of 376

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144340insertion1nstd232human GRCh37.p13 chr14: 95,940,085-95,940,085 , GRCh38.p12 chr14: 95,473,748-95,473,748 SYNE3
    nsv7138302copy number variation1nstd232human GRCh37.p13 chr14: 95,889,841-95,889,942 , GRCh38.p12 chr14: 95,423,504-95,423,605 SYNE3
    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
    nsv7069223inversion1nstd229human GRCh38 chr14: 95,460,643-95,624,077 , GRCh37.p13 chr14: 95,926,980-96,090,414 GLRX5, SNHG10, 5 more genes
    nsv7066649inversion1nstd229human GRCh38 chr14: 95,392,906-95,433,070 , GRCh37.p13 chr14: 95,859,243-95,899,407 SYNE3, LOC105370639, 1 more genes
    nsv6976959copy number variation1nstd229human GRCh38 chr14: 95,425,401-95,434,200 , GRCh37.p13 chr14: 95,891,738-95,900,537 SYNE3
    nsv6976885copy number variation1nstd229human GRCh38 chr14: 95,334,257-95,408,339 , GRCh37.p13 chr14: 95,800,594-95,874,676 LOC105370640, LOC105370639, 4 more genes
    nsv6976837copy number variation1nstd229human GRCh38 chr14: 95,436,399-95,436,626 , GRCh37.p13 chr14: 95,902,736-95,902,963 SYNE3
    nsv6973291copy number variation1nstd229human GRCh38 chr14: 95,376,840-95,459,909 , GRCh37.p13 chr14: 95,843,177-95,926,246 LOC105370640, SYNE3, 1 more genes
    nsv6972807copy number variation1nstd229human GRCh38 chr14: 95,506,801-95,560,700 , GRCh37.p13 chr14: 95,973,138-96,027,037 SCARNA13, GLRX5, 3 more genes
    nsv6970414copy number variation1nstd229human GRCh38 chr14: 95,512,278-95,521,109 , GRCh37.p13 chr14: 95,978,615-95,987,446 SYNE3, SYNE3-AS1
    nsv6968724copy number variation1nstd229human GRCh38 chr14: 95,291,801-95,433,100 , GRCh37.p13 chr14: 95,758,138-95,899,437 LOC107984710, LOC105370638, 6 more genes
    nsv6968411copy number variation1nstd229human GRCh38 chr14: 95,495,655-95,509,942 , GRCh37.p13 chr14: 95,961,992-95,976,279 SYNE3
    nsv6963294copy number variation1nstd229human GRCh38 chr14: 95,329,212-95,499,213 , GRCh37.p13 chr14: 95,795,549-95,965,550 LOC105370639, LOC105370640, 4 more genes
    nsv6960137copy number variation1nstd229human GRCh38 chr14: 95,425,506-95,430,478 , GRCh37.p13 chr14: 95,891,843-95,896,815 SYNE3
    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
    nsv6576769inversion1nstd223human GRCh38 chr14: 95,392,901-95,433,070 , GRCh37.p13 chr14: 95,859,238-95,899,407 SYNE3, LOC105370639, 1 more genes
    nsv6514667copy number variation1nstd223human GRCh38 chr14: 95,486,606-95,487,634 , GRCh37.p13 chr14: 95,952,943-95,953,971 SYNE3
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