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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094373copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,016,689-43,398,220 , GRCh38.p12 chr15: 42,724,491-43,106,022 TTBK2, FDPSP4, 3 more genes
    nsv3891545copy number variation1nstd102humanLikely benign GRCh37 chr15: 43,149,808-43,272,188 , GRCh38.p12 chr15: 42,857,610-42,979,990 TTBK2, FDPSP4, 1 more genes
    nsv6637441copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,051,179-43,261,425 , GRCh38.p12 chr15: 42,758,981-42,969,227 TTBK2, KRT8P50, 2 more genes
    nsv3923593copy number variation1nstd102humanUncertain significance NCBI36 chr15: 40,953,625-41,139,254 , GRCh37.p13 chr15: 43,166,333-43,351,962 , GRCh38.p12 chr15: 42,874,135-43,059,764 TTBK2, FDPSP4, 1 more genes
    nsv7094707copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,164,789-43,270,165 , GRCh38.p12 chr15: 42,872,591-42,977,967 TTBK2, FDPSP4, 1 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 TTBK2, H3P40, 1616 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 TTBK2, RNU6-18P, 1442 more genes
    nsv3903255copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784 TTBK2, RN7SKP101, 234 more genes
    nsv3902367copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436 TTBK2, SERF2-C15ORF63, 142 more genes
    nsv3924334copy number variation1nstd102humanPathogenic GRCh38 chr15: 42,785,627-43,342,260 , GRCh37 chr15: 43,077,825-43,634,458 , NCBI36 chr15: 40,865,117-41,421,750 TTBK2, KRT8P50, 13 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 TTBK2, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 TTBK2, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 TTBK2, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 TTBK2, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 TTBK2, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 TTBK2, RNU6-953P, 1385 more genes
    nsv3899559copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595 TTBK2, CILP, 1176 more genes
    nsv3915997copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 40,646,251-41,926,596 , GRCh37 chr15: 42,858,959-44,139,304 , GRCh38 chr15: 42,566,761-43,847,106 TTBK2, CKMT1B, 46 more genes
    nsv4729554copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,135,272-43,744,542 , GRCh38.p12 chr15: 42,843,074-43,452,344 TTBK2, EPB42, 16 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 TTBK2, SNRPCP18, 1622 more genes
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