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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5522476copy number variation1nstd206human GRCh38 chr15: 74,937,259-74,937,432 , GRCh37.p13 chr15: 75,229,600-75,229,773 COX5A
    nsv5522221copy number variation1nstd206human GRCh38 chr15: 74,921,169-74,922,157 , GRCh37.p13 chr15: 75,213,510-75,214,498 COX5A
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5317453copy number variation1nstd204human GRCh38.p13 chr15: 74,931,810-74,932,914 , GRCh37.p13 chr15: 75,224,151-75,225,255 COX5A
    nsv5306136copy number variation1nstd204human GRCh38.p13 chr15: 74,923,221-74,923,559 , GRCh37.p13 chr15: 75,215,562-75,215,900 COX5A
    nsv5009061copy number variation1nstd200human GRCh38 chr15: 74,938,532-74,942,573 , GRCh37.p13 chr15: 75,230,873-75,234,914 COX5A
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850104copy number variation1nstd200human GRCh37 chr15: 75,224,158-75,225,248 , GRCh38.p12 chr15: 74,931,817-74,932,907 COX5A
    nsv4850103copy number variation1nstd200human GRCh37 chr15: 75,222,280-75,223,159 , GRCh38.p12 chr15: 74,929,939-74,930,818 COX5A
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 FAM219B, MIR4513, 62 more genes
    nsv4675298copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,039,267-75,268,029 , GRCh38.p12 chr15: 74,746,926-74,975,688 SCAMP2, CSK, 11 more genes
    nsv4455940copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183 TBC1D21, CPLX3, 72 more genes
    nsv4455912copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559 MIR6881, ARID3B, 94 more genes
    nsv4455687copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183 SCAMP2, LOC105376731, 74 more genes
    nsv4239653copy number variation1nstd166human GRCh37.p13 chr15: 75,208,264-75,210,270 , GRCh38.p12 chr15: 74,915,923-74,917,929 COX5A
    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
    nsv3920789copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 70,751,023-73,279,197 , GRCh37 chr15: 72,963,970-75,492,144 , GRCh38 chr15: 72,671,629-75,199,803 BBS4, CLK3, 67 more genes
    nsv3920702copy number variation1nstd102humanPathogenic NCBI36 chr15: 70,708,423-73,322,383 , GRCh37 chr15: 72,921,369-75,535,330 , GRCh38 chr15: 72,629,028-75,242,989 FKBP1AP2, EDC3, 73 more genes
    nsv3920020copy number variation1nstd102humanPathogenic GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966 STRA6, LOC105370891, 91 more genes
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