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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6969050copy number variation1nstd229human GRCh38 chr15: 40,229,801-40,497,200 , GRCh37.p13 chr15: 40,522,002-40,789,399 CCDC9B, KNSTRN, 16 more genes
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6309788copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,763,413-40,764,543 , GRCh38.p12 chr15: 40,471,214-40,472,344 CHST14
    nsv6309617copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,763,403-40,764,553 , GRCh38.p12 chr15: 40,471,204-40,472,354 CHST14
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    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
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729095copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,464,942-41,196,807 , GRCh38.p12 chr15: 40,172,741-40,904,609 SPINT1-AS1, KNSTRN, 37 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 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
    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
    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
    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 MIR4513, LOC727751, 1754 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 HDDC3, TRK-CTT16-1, 1622 more genes
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