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Items: 1 to 20 of 246

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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
    nsv5667909inversion1nstd207human GRCh38 chr15: 74,421,627-74,425,871 , GRCh37.p13 chr15: 74,713,968-74,718,212 SEMA7A
    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
    nsv4992334copy number variation1nstd200human GRCh38 chr15: 74,421,828-74,421,931 , GRCh37.p13 chr15: 74,714,169-74,714,272 SEMA7A
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    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
    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
    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
    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 RNU6-18P, GOLGA8K, 1442 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 SNRPCP18, SNORD116-30, 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 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 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 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3915187copy number variation1nstd102humanPathogenic NCBI36 chr15: 70,234,344-100,278,724 , GRCh37 chr15: 72,447,290-102,461,201 , GRCh38 chr15: 72,154,949-101,920,998 LOC102724117, TMEM266, 618 more genes
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