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Items: 1 to 20 of 229

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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
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 LOC105370892, MRPS15P1, 99 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
    nsv7077484inversion1nstd229human GRCh38 chr15: 74,072,224-75,785,570 , GRCh37.p13 chr15: 74,364,565-76,077,911 LOC107984720, SCAMP2, 68 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7066327inversion1nstd229human GRCh38 chr15: 74,062,424-75,303,012 , GRCh37.p13 chr15: 74,354,765-75,595,353 FAM219B, PPCDC, 48 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6974345copy number variation1nstd229human GRCh38 chr15: 74,929,501-74,933,800 , GRCh37.p13 chr15: 75,221,842-75,226,141 COX5A
    nsv6971920copy number variation1nstd229human GRCh38 chr15: 74,924,801-74,927,100 , GRCh37.p13 chr15: 75,217,142-75,219,441 COX5A
    nsv6967803copy number variation1nstd229human GRCh38 chr15: 74,915,912-74,917,950 , GRCh37.p13 chr15: 75,208,253-75,210,291 COX5A
    nsv6966743copy number variation1nstd229human GRCh38 chr15: 74,911,188-74,930,142 , GRCh37.p13 chr15: 75,203,529-75,222,483 COX5A
    nsv6963894copy number variation1nstd229human GRCh38 chr15: 74,936,564-74,936,613 , GRCh37.p13 chr15: 75,228,905-75,228,954 COX5A
    nsv6637763copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,167,794-75,459,288 , GRCh38.p12 chr15: 74,875,453-75,166,947 RPP25, LOC100128721, 5 more genes
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 PTPN9, NRG4, 96 more genes
    nsv6595490inversion1nstd223human GRCh38 chr15: 74,067,732-75,273,464 , GRCh37.p13 chr15: 74,360,073-75,565,805 CCDC33, LOC107984772, 44 more genes
    nsv6594805inversion1nstd223human GRCh38 chr15: 74,067,653-75,273,541 , GRCh37.p13 chr15: 74,359,994-75,565,882 PPCDC, COMMD4P2, 44 more genes
    nsv6592543inversion1nstd223human GRCh38 chr15: 74,064,999-75,300,334 , GRCh37.p13 chr15: 74,357,340-75,592,675 GOLGA6A, MIR6882, 48 more genes
    nsv6506548copy number variation1nstd223human GRCh38 chr15: 74,937,001-74,941,100 , GRCh37.p13 chr15: 75,229,342-75,233,441 COX5A
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