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Items: 1 to 20 of 231

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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
    nsv7077374inversion1nstd229human GRCh38 chr15: 74,978,016-75,592,041 , GRCh37.p13 chr15: 75,270,357-75,884,382 PPCDC, RPL13P4, 21 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
    nsv6976550copy number variation1nstd229human GRCh38 chr15: 75,001,515-75,001,610 , GRCh37.p13 chr15: 75,293,856-75,293,951 SCAMP5
    nsv6966719copy number variation1nstd229human GRCh38 chr15: 75,005,584-75,007,942 , GRCh37.p13 chr15: 75,297,925-75,300,283 SCAMP5
    nsv6961709copy number variation1nstd229human GRCh38 chr15: 74,995,525-74,995,560 , GRCh37.p13 chr15: 75,287,866-75,287,901 SCAMP5
    nsv6960142copy number variation1nstd229human GRCh38 chr15: 75,006,408-75,010,541 , GRCh37.p13 chr15: 75,298,749-75,302,882 SCAMP5
    nsv6959697copy number variation1nstd229human GRCh38 chr15: 75,001,025-75,005,228 , GRCh37.p13 chr15: 75,293,366-75,297,569 SCAMP5
    nsv6959524copy number variation1nstd229human GRCh38 chr15: 75,003,202-75,007,711 , GRCh37.p13 chr15: 75,295,543-75,300,052 SCAMP5
    nsv6958411copy number variation1nstd229human GRCh38 chr15: 75,007,580-75,009,853 , GRCh37.p13 chr15: 75,299,921-75,302,194 SCAMP5
    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
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