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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883741copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 28,149,554-28,151,551 , GRCh38 chr10: 27,860,625-27,862,622 ODAD2
    nsv3873542copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 28,229,332-28,258,434 , GRCh38 chr10: 27,940,403-27,969,505 ODAD2
    nsv5380712copy number variation1nstd102humanUncertain significance GRCh37 chr10: 28,101,421-28,101,574 , GRCh38.p12 chr10: 27,812,492-27,812,645 ODAD2
    nsv4683120copy number variation1nstd102humanPathogenic GRCh37 chr10: 28,223,929-28,288,977 , GRCh38.p12 chr10: 27,935,000-28,000,048 LOC112268060, ODAD2
    nsv3873913copy number variation1nstd102humanPathogenic GRCh38 chr10: 27,981,131-27,986,391 , GRCh37 chr10: 28,270,060-28,275,320 ODAD2, LOC112268060
    nsv5380713copy number variation1nstd102humanUncertain significance GRCh37 chr10: 28,101,421-28,250,664 , GRCh38.p12 chr10: 27,812,492-27,961,735 RPL36AP55, ODAD2
    nsv3899502copy number variation1nstd102humanBenign GRCh37 chr10: 27,975,180-28,141,445 , GRCh38.p12 chr10: 27,686,251-27,852,516 MKX, MKX-AS1, 2 more genes
    nsv3919475copy number variation1nstd102humanUncertain significance NCBI36 chr10: 28,185,206-28,366,388 , GRCh37.p13 chr10: 28,145,200-28,326,382 , GRCh38.p12 chr10: 27,856,271-28,037,453 LOC112268060, ODAD2, 2 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv3911283copy number variation1nstd102humanPathogenic GRCh37 chr10: 27,111,945-30,537,855 , NCBI36 chr10: 27,151,951-30,577,861 , GRCh38 chr10: 26,823,016-30,248,926 YME1L1, SVIL, 72 more genes
    nsv3915584copy number variation1nstd102humanPathogenic GRCh38 chr10: 27,046,685-30,228,891 , GRCh37 chr10: 27,335,614-30,517,820 , NCBI36 chr10: 27,375,620-30,557,826 TRIAP1P1, LOC112268060, 70 more genes
    nsv6291211copy number variation1nstd102humanPathogenic GRCh37 chr10: 27,204,530-29,105,882 , GRCh38.p12 chr10: 26,915,601-28,816,953 LINC02673, FAM210CP, 44 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 LINC00700, LINC02881, 806 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
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