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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
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5938972copy number variation1nstd209human GRCh38 chr15: 95,301,994-96,435,598 , GRCh37.p13 chr15: 95,845,223-96,978,828 , RNU2-3P, 13 more genes
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4619556copy number variation1nstd183human GRCh37 chr15: 96,873,503-96,874,703 , GRCh38.p12 chr15: 96,330,274-96,331,474 MIR1469, NR2F2
    nsv4578637copy number variation1nstd102humanPathogenic GRCh37 chr15: 96,878,099-102,397,836 , GRCh38.p12 chr15: 96,334,870-101,857,633 SYNM-AS1, LINC02253, 94 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4419166copy number variation1nstd174human GRCh37 chr15: 96,873,212-96,874,703 , GRCh38.p12 chr15: 96,329,983-96,331,474 NR2F2, MIR1469
    nsv4350607copy number variation1nstd102humanPathogenic GRCh37 chr15: 96,873,212-102,389,423 , GRCh38.p12 chr15: 96,329,983-101,849,220 LOC105371010, SELENOS, 95 more genes
    nsv3924639copy number variation1nstd102humanPathogenic GRCh37 chr15: 94,576,237-102,383,473 , NCBI36 chr15: 92,377,241-100,200,996 , GRCh38 chr15: 94,033,008-101,843,270 RNU6-807P, LETR1, 119 more genes
    nsv3924570copy number variation1nstd102humanLikely benign NCBI36 chr15: 94,439,534-94,982,999 , GRCh37.p13 chr15: 96,638,530-97,181,995 , GRCh38.p12 chr15: 96,095,301-96,638,765 TUBAP12, RPL31P55, 10 more genes
    nsv3923265copy number variation1nstd102humanPathogenic GRCh37 chr15: 96,567,356-102,461,201 , NCBI36 chr15: 94,368,360-100,278,724 , GRCh38 chr15: 96,024,127-101,920,998 LOC107987228, ARRDC4, 104 more genes
    nsv3922914copy number variation1nstd102humanPathogenic NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189 OR4F14P, RNA5SP401, 124 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3921313copy number variation1nstd102humanPathogenic GRCh37 chr15: 96,313,856-102,351,195 , NCBI36 chr15: 94,114,860-100,168,718 , GRCh38 chr15: 95,770,627-101,810,992 SELENOS, SPATA8-AS1, 97 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
    nsv3920248copy number variation1nstd102humanPathogenic NCBI36 chr15: 87,618,716-100,262,146 , GRCh37.p13 chr15: 89,817,712-102,444,623 , GRCh38.p12 chr15: 89,274,481-101,904,420 FAM149B1P1, MIR9-3HG, 229 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919393copy number variation1nstd102humanPathogenic NCBI36 chr15: 84,170,900-100,278,724 , GRCh37 chr15: 86,369,896-102,461,201 , GRCh38 chr15: 85,826,665-101,920,998 LOC105370997, LOC102724465, 270 more genes
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