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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
    nsv4629919copy number variation1nstd183human GRCh37 chr15: 50,647,043-50,648,067 , GRCh38.p12 chr15: 50,354,846-50,355,870 GABPB1-IT1, GABPB1, 1 more genes
    nsv4625654copy number variation1nstd183human GRCh37 chr15: 50,642,732-50,648,067 , GRCh38.p12 chr15: 50,350,535-50,355,870 GABPB1-IT1, GABPB1, 1 more genes
    nsv4456655copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,083,229-53,439,931 , GRCh38.p12 chr15: 49,791,032-53,147,734 CERNA1, MAPK6-DT, 64 more genes
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4455359copy number variation1nstd102humanPathogenic GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199 MIR4716, RPS13P8, 112 more genes
    nsv4376200copy number variation1nstd173human GRCh37 chr15: 50,612,734-50,681,680 , GRCh38.p12 chr15: 50,320,537-50,389,483 GABPB1-AS1, MIR4712, 3 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
    nsv3917643copy number variation1nstd102humanPathogenic GRCh38 chr15: 47,460,844-52,494,222 , GRCh37 chr15: 47,753,041-52,786,419 , NCBI36 chr15: 45,540,333-50,573,711 LOC105370819, TMOD2, 86 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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