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Items: 1 to 20 of 319

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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
    nsv7068575inversion1nstd229human GRCh38 chr14: 34,940,464-35,091,648 , GRCh37.p13 chr14: 35,409,670-35,560,854 PPP2R3C, IGBP1P1, 4 more genes
    nsv6957562copy number variation1nstd229human GRCh38 chr14: 34,796,766-35,163,366 , GRCh37.p13 chr14: 35,265,972-35,632,572 PRORP, FAM177A1, 10 more genes
    nsv6955674copy number variation1nstd229human GRCh38 chr14: 34,311,401-35,159,200 , GRCh37.p13 chr14: 34,780,607-35,628,406 SRP54, SPTSSA, 26 more genes
    nsv6955641copy number variation1nstd229human GRCh38 chr14: 34,924,660-35,315,430 , GRCh37.p13 chr14: 35,393,866-35,784,636 PRORP, IGBP1P1, 12 more genes
    nsv6952326copy number variation1nstd229human GRCh38 chr14: 35,112,354-35,120,128 , GRCh37.p13 chr14: 35,581,560-35,589,334 LOC101927178, PPP2R3C
    nsv6950397copy number variation1nstd229human GRCh38 chr14: 35,118,278-35,229,922 , GRCh37.p13 chr14: 35,587,484-35,699,128 PRORP, RPL23AP70, 4 more genes
    nsv6948128copy number variation1nstd229human GRCh38 chr14: 35,117,284-35,119,889 , GRCh37.p13 chr14: 35,586,490-35,589,095 PPP2R3C
    nsv6947463copy number variation1nstd229human GRCh38 chr14: 35,092,613-35,141,668 , GRCh37.p13 chr14: 35,561,819-35,610,874 LOC101927178, PPP2R3C, 1 more genes
    nsv6946833copy number variation1nstd229human GRCh38 chr14: 35,058,701-35,233,100 , GRCh37.p13 chr14: 35,527,907-35,702,306 DPRXP3, LOC101927178, 6 more genes
    nsv6946013copy number variation1nstd229human GRCh38 chr14: 35,083,523-35,084,656 , GRCh37.p13 chr14: 35,552,729-35,553,862 LOC101927178, PPP2R3C, 1 more genes
    nsv6945702copy number variation1nstd229human GRCh38 chr14: 35,100,202-35,178,934 , GRCh37.p13 chr14: 35,569,408-35,648,140 PRORP, SEPTIN7P1, 3 more genes
    nsv6945119copy number variation1nstd229human GRCh38 chr14: 35,061,277-35,087,342 , GRCh37.p13 chr14: 35,530,483-35,556,548 FAM177A1, LOC101927178, 1 more genes
    nsv6943128copy number variation1nstd229human GRCh38 chr14: 35,083,301-35,133,600 , GRCh37.p13 chr14: 35,552,507-35,602,806 PPP2R3C, PRORP, 2 more genes
    nsv6939728copy number variation1nstd229human GRCh38 chr14: 34,836,903-35,282,666 , GRCh37.p13 chr14: 35,306,109-35,751,872 SEPTIN7P1, SRP54-AS1, 15 more genes
    nsv6939686copy number variation1nstd229human GRCh38 chr14: 35,092,063-35,297,461 , GRCh37.p13 chr14: 35,561,269-35,766,667 PRORP, PSMA6, 8 more genes
    nsv6622711copy number variation1nstd224human GRCh37 chr14: 35,542,146-35,715,411 , GRCh38.p12 chr14: 35,072,940-35,246,205 PRORP, PPP2R3C, 7 more genes
    nsv6622631copy number variation1nstd224human GRCh37 chr14: 35,554,859-35,579,746 , GRCh38.p12 chr14: 35,085,653-35,110,540 PPP2R3C, LOC101927178
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