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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940957copy number variation1nstd209human GRCh38 chr15: 42,496,457-42,496,591 , GRCh37.p13 chr15: 42,788,655-42,788,789 SNAP23
    nsv5935475copy number variation1nstd209human GRCh38 chr15: 42,490,161-42,490,557 , GRCh37.p13 chr15: 42,782,359-42,782,755 SNAP23, ZNF106
    nsv5729498mobile element insertion2nstd211human GRCh38 chr15: 42,514,141-42,514,141 , GRCh37.p13 chr15: 42,806,339-42,806,339 SNAP23
    nsv5701842mobile element insertion1nstd211human GRCh38 chr15: 42,522,716-42,522,716 , GRCh37.p13 chr15: 42,814,914-42,814,914 SNAP23
    nsv5663211insertion1nstd207human GRCh38 chr15: 42,514,126-42,514,126 , GRCh37.p13 chr15: 42,806,324-42,806,324 SNAP23
    nsv5654881insertion1nstd207human GRCh38 chr15: 42,518,940-42,518,940 , GRCh37.p13 chr15: 42,811,138-42,811,138 SNAP23
    nsv5562201mobile element insertion1nstd206human GRCh38 chr15: 42,514,141-42,514,143 , GRCh37.p13 chr15: 42,806,339-42,806,341 SNAP23
    nsv5508562copy number variation1nstd206human GRCh38 chr15: 42,520,512-42,525,506 , GRCh37.p13 chr15: 42,812,710-42,817,704 SNAP23
    nsv5499785copy number variation1nstd206human GRCh38 chr15: 42,490,165-42,490,558 , GRCh37.p13 chr15: 42,782,363-42,782,756 ZNF106, SNAP23
    nsv5497720copy number variation1nstd206human GRCh38 chr15: 42,514,852-42,525,650 , GRCh37.p13 chr15: 42,807,050-42,817,848 SNAP23
    nsv5497322copy number variation1nstd206human GRCh38 chr15: 42,496,457-42,496,604 , GRCh37.p13 chr15: 42,788,655-42,788,802 SNAP23
    nsv5497086copy number variation1nstd206human GRCh38 chr15: 42,507,887-42,508,564 , GRCh37.p13 chr15: 42,800,085-42,800,762 SNAP23
    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
    nsv5366919translocation1nstd200human GRCh38 chr15: 42,532,827-42,532,827 , GRCh38 chr2: 241,370,547-241,370,547 , GRCh37.p13 chr15: 42,825,025-42,825,025 , GRCh37.p13 chr2: 242,309,962-242,309,962 SNAP23, FARP2, 2 more genes
    nsv5357857translocation1nstd200human GRCh38 chr15: 42,490,165-42,490,165 , GRCh38 chr15: 42,490,558-42,490,558 , GRCh37.p13 chr15: 42,782,756-42,782,756 , GRCh37.p13 chr15: 42,782,363-42,782,363 ZNF106, SNAP23
    nsv5341191translocation1nstd200human GRCh37 chr15: 42,782,363-42,782,363 , GRCh37 chr15: 42,782,756-42,782,756 , GRCh38.p12 chr15: 42,490,165-42,490,165 , GRCh38.p12 chr15: 42,490,558-42,490,558 ZNF106, SNAP23
    nsv5330780translocation1nstd200human GRCh37 chr2: 242,309,962-242,309,962 , GRCh37 chr15: 42,825,025-42,825,025 , GRCh38.p12 chr15: 42,532,827-42,532,827 , GRCh38.p12 chr2: 241,370,547-241,370,547 SNAP23, FARP2, 2 more genes
    nsv5300704copy number variation1nstd204human GRCh38.p13 chr15: 42,488,703-42,490,533 , GRCh37.p13 chr15: 42,780,901-42,782,731 SNAP23, ZNF106
    nsv5271745copy number variation1nstd204human GRCh38.p13 chr15: 42,492,123-42,493,438 , GRCh37.p13 chr15: 42,784,321-42,785,636 SNAP23
    nsv5189978mobile element insertion1nstd203human GRCh38 chr15: 42,514,126-42,514,141 , GRCh37.p13 chr15: 42,806,324-42,806,339 SNAP23
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