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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 CCNDBP1, 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 CCNDBP1, 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 CCNDBP1, RN7SKP101, 234 more genes
    nsv3902367copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436 CCNDBP1, 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 CCNDBP1, KRT8P50, 13 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 CCNDBP1, 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 CCNDBP1, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 CCNDBP1, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 CCNDBP1, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 CCNDBP1, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 CCNDBP1, 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 CCNDBP1, 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 CCNDBP1, 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 CCNDBP1, 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 CCNDBP1, SNRPCP18, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 CCNDBP1, SNORD116-23, 1622 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 CCNDBP1, PPIP5K1P1-CATSPER2, 44 more genes
    nsv4457111copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,062,580-43,744,411 , GRCh38.p12 chr15: 42,770,382-43,452,213 CCNDBP1, TUBGCP4, 17 more genes
    nsv4456301copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,062,580-43,737,484 , GRCh38.p12 chr15: 42,770,382-43,445,286 CCNDBP1, LCMT2, 17 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 CCNDBP1, HDDC3, 1622 more genes
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