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Items: 1 to 20 of 158

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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
    nsv5929984copy number variation1nstd209human GRCh38 chr15: 74,903,545-74,903,622 , GRCh37.p13 chr15: 75,195,886-75,195,963 FAM219B
    nsv5672749copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 75,188,483-75,190,081 , GRCh38.p12 chr15: 74,896,142-74,897,740 MPI, FAM219B
    nsv5516522copy number variation1nstd206human GRCh38 chr15: 74,903,583-74,903,639 , GRCh37.p13 chr15: 75,195,924-75,195,980 FAM219B
    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
    nsv5265043copy number variation1nstd204human GRCh38.p13 chr15: 74,898,313-74,899,762 , GRCh37.p13 chr15: 75,190,654-75,192,103 MPI, FAM219B
    nsv5264751copy number variation1nstd204human GRCh38.p13 chr15: 74,898,763-74,899,762 , GRCh37.p13 chr15: 75,191,104-75,192,103 MPI, FAM219B
    nsv5009057copy number variation1nstd200human GRCh38 chr15: 74,796,648-74,914,092 , GRCh37.p13 chr15: 75,088,989-75,206,433 CSK, SCAMP2, 7 more genes
    nsv5001758copy number variation1nstd200human GRCh38 chr15: 74,901,740-74,902,867 , GRCh37.p13 chr15: 75,194,081-75,195,208 FAM219B, MPI
    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
    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
    nsv4249025copy number variation1nstd166human GRCh37.p13 chr15: 75,191,160-75,192,093 , GRCh38.p12 chr15: 74,898,819-74,899,752 FAM219B, MPI
    nsv4240750copy number variation1nstd166human GRCh37.p13 chr15: 75,200,012-75,206,749 , GRCh38.p12 chr15: 74,907,671-74,914,408 FAM219B
    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
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