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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7094312copy number variation2nstd102humanUncertain significance GRCh37 chr15: 89,379,429-91,565,479 , GRCh38.p12 chr15: 88,836,198-91,022,249 IQGAP1, WDR93, 77 more genes
    nsv7068128inversion1nstd229human GRCh38 chr15: 87,287,023-90,484,635 , GRCh37.p13 chr15: 87,830,254-91,027,867 , LOC105370964, 81 more genes
    nsv7065612inversion1nstd229human GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970 ZNF774, CRAT37, 77 more genes
    nsv7062993inversion1nstd229human GRCh38 chr15: 85,570,479-90,463,746 , GRCh37.p13 chr15: 86,113,710-91,006,978 , NTRK3-AS1, 97 more genes
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6976297copy number variation1nstd229human GRCh38 chr15: 90,103,707-90,300,544 , GRCh37.p13 chr15: 90,646,939-90,843,776 RN7SL736P, IDH2-DT, 9 more genes
    nsv6973320copy number variation1nstd229human GRCh38 chr15: 90,188,237-90,607,645 , GRCh37.p13 chr15: 90,731,469-91,150,877 CIB1, NIFKP5, 12 more genes
    nsv6972556copy number variation1nstd229human GRCh38 chr15: 90,266,400-90,271,186 , GRCh37.p13 chr15: 90,809,632-90,814,418 NGRN
    nsv6972037copy number variation1nstd229human GRCh38 chr15: 90,269,761-90,300,154 , GRCh37.p13 chr15: 90,812,993-90,843,386 RN7SL736P, NGRN, 2 more genes
    nsv6970650copy number variation1nstd229human GRCh38 chr15: 90,263,949-90,266,359 , GRCh37.p13 chr15: 90,807,181-90,809,591 NGRN, CIB1
    nsv6969395copy number variation1nstd229human GRCh38 chr15: 90,252,190-90,302,122 , GRCh37.p13 chr15: 90,795,422-90,845,354 RN7SL736P, TTLL13, 4 more genes
    nsv6961996copy number variation1nstd229human GRCh38 chr15: 90,197,716-90,286,436 , GRCh37.p13 chr15: 90,740,948-90,829,668 SEMA4B, GDPGP1, 5 more genes
    nsv6960807copy number variation1nstd229human GRCh38 chr15: 89,944,292-90,294,853 , GRCh37.p13 chr15: 90,487,524-90,838,085 ZNF710-AS1, RN7SL346P, 13 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6623355copy number variation1nstd224human GRCh37 chr15: 90,814,420-90,838,393 , GRCh38.p12 chr15: 90,271,188-90,295,161 GOLGA2P8, NIFKP5, 2 more genes
    nsv6582041inversion1nstd223human GRCh38 chr15: 85,570,476-90,463,749 , GRCh37.p13 chr15: 86,113,707-91,006,981 , AP3S2, 97 more genes
    nsv6511416copy number variation1nstd223human GRCh38 chr15: 90,269,761-90,300,150 , GRCh37.p13 chr15: 90,812,993-90,843,382 GOLGA2P8, NIFKP5, 2 more genes
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