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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937108copy number variation1nstd209human GRCh38 chr19: 45,721,775-45,721,827 , GRCh37.p13 chr19: 46,225,033-46,225,085 FBXO46
    nsv5728965mobile element insertion1nstd211human GRCh38 chr19: 45,718,942-45,718,942 , GRCh37.p13 chr19: 46,222,200-46,222,200 FBXO46
    nsv5700761mobile element insertion1nstd211human GRCh38 chr19: 45,718,961-45,718,961 , GRCh37.p13 chr19: 46,222,219-46,222,219 FBXO46
    nsv5697896mobile element insertion1nstd211human GRCh38 chr19: 45,732,413-45,732,413 , GRCh37.p13 chr19: 46,235,671-46,235,671 MEIOSIN, FBXO46
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5523275copy number variation1nstd206human GRCh38 chr19: 45,713,967-45,714,083 , GRCh37.p13 chr19: 46,217,225-46,217,341 FBXO46
    nsv5521641copy number variation1nstd206human GRCh38 chr19: 45,721,776-45,721,828 , GRCh37.p13 chr19: 46,225,034-46,225,086 FBXO46
    nsv5515792copy number variation1nstd206human GRCh38 chr19: 45,704,606-45,709,612 , GRCh37.p13 chr19: 46,207,864-46,212,870 FBXO46
    nsv5428846mobile element insertion1nstd206human GRCh38 chr19: 45,732,427-45,732,462 , GRCh37.p13 chr19: 46,235,685-46,235,720 MEIOSIN, FBXO46
    nsv5359845translocation1nstd200human GRCh38 chr19: 45,713,967-45,713,967 , GRCh38 chr19: 45,714,083-45,714,083 , GRCh37.p13 chr19: 46,217,225-46,217,225 , GRCh37.p13 chr19: 46,217,341-46,217,341 FBXO46
    nsv5327341copy number variation1nstd204human GRCh38.p13 chr19: 45,584,936-45,884,300 , GRCh37.p13 chr19: 46,088,194-46,387,558 DMWD, GPR4, 19 more genes
    nsv5324913copy number variation1nstd204human GRCh38.p13 chr19: 45,713,959-45,714,091 , GRCh37.p13 chr19: 46,217,217-46,217,349 FBXO46
    nsv5295867copy number variation1nstd204human GRCh38.p13 chr19: 45,722,001-45,723,900 , GRCh37.p13 chr19: 46,225,259-46,227,158 FBXO46
    nsv5294394copy number variation1nstd204human GRCh38.p13 chr19: 45,726,826-45,742,477 , GRCh37.p13 chr19: 46,230,084-46,245,735 MEIOSIN, FBXO46
    nsv5293027copy number variation1nstd204human GRCh38.p13 chr19: 45,712,214-45,721,402 , GRCh37.p13 chr19: 46,215,472-46,224,660 FBXO46
    nsv5284788copy number variation1nstd204human GRCh38.p13 chr19: 45,504,601-45,776,400 , GRCh37.p13 chr19: 46,007,859-46,279,658 MIR642A, LOC107985315, 17 more genes
    nsv5192676mobile element insertion1nstd203human GRCh38 chr19: 45,732,413-45,732,413 , GRCh37.p13 chr19: 46,235,671-46,235,671 FBXO46, MEIOSIN
    nsv5024731copy number variation1nstd200human GRCh38 chr19: 45,652,324-45,724,747 , GRCh37.p13 chr19: 46,155,582-46,228,005 QPCTL, MIR642A, 4 more genes
    nsv5020714copy number variation1nstd200human GRCh38 chr19: 45,722,055-45,723,819 , GRCh37.p13 chr19: 46,225,313-46,227,077 FBXO46
    nsv4865213copy number variation1nstd200human GRCh37 chr19: 46,207,864-46,212,870 , GRCh38.p12 chr19: 45,704,606-45,709,612 FBXO46
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