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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939896copy number variation1nstd209human GRCh38 chr19: 48,935,690-48,959,222 , GRCh37.p13 chr19: 49,438,947-49,462,479 BAX, DHDH
    nsv5935755copy number variation1nstd209human GRCh38 chr19: 48,929,835-48,936,990 , GRCh37.p13 chr19: 49,433,092-49,440,247 DHDH
    nsv5931624copy number variation1nstd209human GRCh38 chr19: 48,938,727-48,942,088 , GRCh37.p13 chr19: 49,441,984-49,445,345 DHDH
    nsv5929190copy number variation1nstd209human GRCh38 chr19: 48,940,457-48,940,903 , GRCh37.p13 chr19: 49,443,714-49,444,160 DHDH
    nsv5879319copy number variation1nstd209human GRCh38 chr19: 48,930,719-48,932,118 , GRCh37.p13 chr19: 49,433,976-49,435,375 DHDH
    nsv5878414copy number variation2nstd209human GRCh38 chr19: 48,934,196-48,937,081 , GRCh37.p13 chr19: 49,437,453-49,440,338 DHDH
    nsv5877334copy number variation2nstd209human GRCh38 chr19: 48,938,670-48,942,112 , GRCh37.p13 chr19: 49,441,927-49,445,369 DHDH
    nsv5868039copy number variation1nstd209human GRCh38 chr19: 48,938,520-48,955,986 , GRCh37.p13 chr19: 49,441,777-49,459,243 BAX, DHDH
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5662603insertion1nstd207human GRCh38 chr19: 48,940,457-48,940,457 , GRCh37.p13 chr19: 49,443,714-49,443,714 DHDH
    nsv5527553copy number variation1nstd206human GRCh38 chr19: 48,935,497-48,937,808 , GRCh37.p13 chr19: 49,438,754-49,441,065 DHDH
    nsv5524247copy number variation1nstd206human GRCh38 chr19: 48,929,728-48,937,034 , GRCh37.p13 chr19: 49,432,985-49,440,291 DHDH
    nsv5514148copy number variation1nstd206human GRCh38 chr19: 48,940,457-48,940,906 , GRCh37.p13 chr19: 49,443,714-49,444,163 DHDH
    nsv5380290translocation1nstd200human GRCh38 chr19: 48,937,770-48,937,770 , GRCh38 chr19: 48,935,496-48,935,496 , GRCh37.p13 chr19: 49,441,027-49,441,027 , GRCh37.p13 chr19: 49,438,753-49,438,753 DHDH
    nsv5296367copy number variation1nstd204human GRCh38.p13 chr19: 48,935,696-48,937,719 , GRCh37.p13 chr19: 49,438,953-49,440,976 DHDH
    nsv5160284mobile element insertion1nstd203human GRCh38 chr19: 48,935,877-48,935,891 , GRCh37.p13 chr19: 49,439,134-49,439,148 DHDH
    nsv5024800copy number variation1nstd200human GRCh38 chr19: 48,931,868-48,935,588 , GRCh37.p13 chr19: 49,435,125-49,438,845 DHDH
    nsv4853298copy number variation1nstd200human GRCh37 chr19: 49,441,954-49,445,350 , GRCh38.p12 chr19: 48,938,697-48,942,093 DHDH
    nsv4853297copy number variation1nstd200human GRCh37 chr19: 49,438,746-49,440,994 , GRCh38.p12 chr19: 48,935,489-48,937,737 DHDH
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
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