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Items: 1 to 20 of 263

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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
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7063009inversion1nstd229human GRCh38 chr15: 80,220,949-81,163,179 , GRCh37.p13 chr15: 80,513,291-81,455,520 CEMIP, ARNT2, 13 more genes
    nsv6976069copy number variation1nstd229human GRCh38 chr15: 80,624,801-80,751,800 , GRCh37.p13 chr15: 80,917,142-81,044,141 RNU6-380P, ABHD17C
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6968998copy number variation1nstd229human GRCh38 chr15: 80,715,081-80,715,409 , GRCh37.p13 chr15: 81,007,422-81,007,750 ABHD17C
    nsv6960621copy number variation1nstd229human GRCh38 chr15: 80,733,332-80,738,803 , GRCh37.p13 chr15: 81,025,673-81,031,144 ABHD17C
    nsv6959196copy number variation1nstd229human GRCh38 chr15: 80,745,190-80,748,241 , GRCh37.p13 chr15: 81,037,531-81,040,582 ABHD17C
    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
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 more genes
    nsv6579530inversion1nstd223human GRCh38 chr15: 77,618,605-83,035,894 , GRCh37.p13 chr15: 77,910,947-83,704,646 CIB2, TFDP1P3, 127 more genes
    nsv6579525inversion1nstd223human GRCh38 chr15: 77,618,608-83,164,280 , GRCh37.p13 chr15: 77,910,950-83,833,032 STARD5, RPL9P8, 131 more genes
    nsv6579316inversion1nstd223human GRCh38 chr15: 80,355,809-82,694,011 , GRCh37.p13 chr15: 80,648,151-83,362,763 MIR549A, RPS17, 46 more genes
    nsv6578911inversion1nstd223human GRCh38 chr15: 77,618,608-84,708,062 , GRCh37.p13 chr15: 77,910,950-85,251,293 TMC3-AS1, LOC642677, 177 more genes
    nsv6511319copy number variation1nstd223human GRCh38 chr15: 80,721,059-80,724,071 , GRCh37.p13 chr15: 81,013,400-81,016,412 ABHD17C
    nsv6504859copy number variation1nstd223human GRCh38 chr15: 80,717,597-80,719,482 , GRCh37.p13 chr15: 81,009,938-81,011,823 ABHD17C
    nsv6497480copy number variation1nstd223human GRCh38 chr15: 80,694,001-80,698,100 , GRCh37.p13 chr15: 80,986,342-80,990,441 ABHD17C
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