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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290450copy number variation1nstd102humanUncertain significance GRCh38 chr15: 51,681,311-51,791,472 , GRCh37.p13 chr15: 51,973,508-52,083,669 LYSMD2, TMOD2, 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 LYSMD2, 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 LYSMD2, 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 LYSMD2, RN7SKP101, 234 more genes
    nsv3903669copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043 LYSMD2, MIR4712, 188 more genes
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 LYSMD2, PYGO1, 125 more genes
    nsv3913164copy number variation1nstd102humanPathogenic GRCh38 chr15: 50,864,913-59,646,577 , GRCh37 chr15: 51,157,110-59,938,776 , NCBI36 chr15: 48,944,402-57,726,068 LYSMD2, LOC112268148, 131 more genes
    nsv3910893copy number variation1nstd102humanPathogenic NCBI36 chr15: 49,356,179-55,167,876 , GRCh37 chr15: 51,568,887-57,380,584 , GRCh38 chr15: 51,276,690-57,088,386 LYSMD2, MAPK6-DT, 76 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 LYSMD2, BCL2L10, 86 more genes
    nsv3917643copy number variation1nstd102humanPathogenic GRCh38 chr15: 47,460,844-52,494,222 , GRCh37 chr15: 47,753,041-52,786,419 , NCBI36 chr15: 45,540,333-50,573,711 LYSMD2, LOC105370819, 86 more genes
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LYSMD2, LOC105370826, 48 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 LYSMD2, 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 LYSMD2, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 LYSMD2, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 LYSMD2, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 LYSMD2, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 LYSMD2, 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 LYSMD2, CILP, 1176 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LYSMD2, LINC03065, 228 more genes
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 LYSMD2, MIR1266, 199 more genes
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