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Items: 1 to 20 of 855

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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
    nsv6957917copy number variation1nstd229human GRCh38 chr14: 35,180,756-35,222,930 , GRCh37.p13 chr14: 35,649,962-35,692,136 DPRXP3, MRPL57P8, 1 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
    nsv6956571copy number variation1nstd229human GRCh38 chr14: 35,196,538-35,199,756 , GRCh37.p13 chr14: 35,665,744-35,668,962 PRORP
    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
    nsv6954184copy number variation1nstd229human GRCh38 chr14: 35,206,761-35,209,476 , GRCh37.p13 chr14: 35,675,967-35,678,682 PRORP
    nsv6953181copy number variation1nstd229human GRCh38 chr14: 35,133,601-35,145,300 , GRCh37.p13 chr14: 35,602,807-35,614,506 PRORP, RPL23AP70
    nsv6953081copy number variation1nstd229human GRCh38 chr14: 35,273,380-35,276,916 , GRCh37.p13 chr14: 35,742,586-35,746,122 PRORP, PSMA6
    nsv6953080copy number variation1nstd229human GRCh38 chr14: 35,172,896-35,186,664 , GRCh37.p13 chr14: 35,642,102-35,655,870 PRORP
    nsv6952796copy number variation1nstd229human GRCh38 chr14: 35,138,852-35,194,535 , GRCh37.p13 chr14: 35,608,058-35,663,741 PRORP, SEPTIN7P1, 1 more genes
    nsv6951476copy number variation1nstd229human GRCh38 chr14: 35,132,734-35,133,394 , GRCh37.p13 chr14: 35,601,940-35,602,600 PRORP
    nsv6951196copy number variation1nstd229human GRCh38 chr14: 35,267,685-35,279,405 , GRCh37.p13 chr14: 35,736,891-35,748,611 PRORP, PSMA6
    nsv6951170copy number variation1nstd229human GRCh38 chr14: 35,270,853-35,278,270 , GRCh37.p13 chr14: 35,740,059-35,747,476 PRORP, PSMA6
    nsv6951055copy number variation1nstd229human GRCh38 chr14: 35,237,901-35,244,800 , GRCh37.p13 chr14: 35,707,107-35,714,006 PRORP
    nsv6950956copy number variation1nstd229human GRCh38 chr14: 35,260,457-35,263,259 , GRCh37.p13 chr14: 35,729,663-35,732,465 PRORP, RPL9P3
    nsv6950657copy number variation1nstd229human GRCh38 chr14: 35,136,422-35,145,877 , GRCh37.p13 chr14: 35,605,628-35,615,083 PRORP, RPL23AP70
    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
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