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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978240insertion1nstd209human GRCh38 chr14: 30,439,539-30,439,539 , GRCh37.p13 chr14: 30,908,745-30,908,745 G2E3-AS1, LOC112267868
    nsv5939188copy number variation1nstd209human GRCh38 chr14: 29,781,060-30,479,820 , GRCh37.p13 chr14: 30,250,266-30,949,026 PRKD1, RPS6P24, 5 more genes
    nsv5928002copy number variation1nstd209human GRCh38 chr14: 30,517,301-30,517,547 , GRCh37.p13 chr14: 30,986,507-30,986,753 G2E3-AS1, LOC112267868
    nsv5708173mobile element insertion1nstd211human GRCh38 chr14: 30,541,036-30,541,036 , GRCh37.p13 chr14: 31,010,242-31,010,242 SYF2P1, G2E3-AS1, 1 more genes
    nsv5702277mobile element insertion2nstd211human GRCh38 chr14: 30,465,403-30,465,403 , GRCh37.p13 chr14: 30,934,609-30,934,609 G2E3-AS1, LOC112267868
    nsv5596944copy number variation1nstd207human GRCh38 chr14: 30,517,305-30,517,551 , GRCh37.p13 chr14: 30,986,511-30,986,757 LOC112267868, G2E3-AS1
    nsv5512907copy number variation1nstd206human GRCh38 chr14: 30,517,301-30,517,555 , GRCh37.p13 chr14: 30,986,507-30,986,761 G2E3-AS1, LOC112267868
    nsv5512433copy number variation1nstd206human GRCh38 chr14: 30,520,098-30,521,508 , GRCh37.p13 chr14: 30,989,304-30,990,714 G2E3-AS1, LOC112267868
    nsv5505506copy number variation1nstd206human GRCh38 chr14: 30,521,435-30,522,006 , GRCh37.p13 chr14: 30,990,641-30,991,212 LOC112267868, G2E3-AS1
    nsv5502441copy number variation1nstd206human GRCh38 chr14: 30,491,829-30,492,123 , GRCh37.p13 chr14: 30,961,035-30,961,329 G2E3-AS1, LOC112267868
    nsv5498696copy number variation1nstd206human GRCh38 chr14: 30,485,812-30,492,601 , GRCh37.p13 chr14: 30,955,018-30,961,807 G2E3-AS1, LOC112267868
    nsv5495824copy number variation1nstd206human GRCh38 chr14: 30,558,601-30,558,678 , GRCh37.p13 chr14: 31,027,807-31,027,884 G2E3, G2E3-AS1
    nsv5430406mobile element insertion1nstd206human GRCh38 chr14: 30,465,403-30,465,454 , GRCh37.p13 chr14: 30,934,609-30,934,660 G2E3-AS1, LOC112267868
    nsv5381770copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,450,705-31,529,481 , GRCh38.p12 chr14: 26,981,499-31,060,275 RPS27AP4, LINC00645, 43 more genes
    nsv5374474translocation1nstd200human GRCh38 chr14: 30,492,579-30,492,579 , GRCh38 chr14: 30,485,834-30,485,834 , GRCh37.p13 chr14: 30,961,785-30,961,785 , GRCh37.p13 chr14: 30,955,040-30,955,040 G2E3-AS1, LOC112267868
    nsv5319216copy number variation1nstd204human GRCh37.p13 chr14: 30,986,507-30,986,761 , GRCh38.p13 chr14: 30,517,301-30,517,555 G2E3-AS1, LOC112267868
    nsv5314394copy number variation1nstd204human GRCh38.p13 chr14: 30,508,145-30,527,067 , GRCh37.p13 chr14: 30,977,351-30,996,273 LOC112267868, LOC105370432, 1 more genes
    nsv5271825copy number variation1nstd204human GRCh38.p13 chr14: 30,507,633-30,527,007 , GRCh37.p13 chr14: 30,976,839-30,996,213 LOC112267868, G2E3-AS1, 1 more genes
    nsv5262979copy number variation1nstd204human GRCh38.p13 chr14: 30,517,301-30,517,500 , GRCh37.p13 chr14: 30,986,507-30,986,706 LOC112267868, G2E3-AS1
    nsv5155952mobile element insertion1nstd203human GRCh38 chr14: 30,508,351-30,508,367 , GRCh37.p13 chr14: 30,977,557-30,977,573 G2E3-AS1, LOC105370432, 1 more genes
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