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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869644copy number variation1nstd209human GRCh38 chr19: 10,541,482-10,543,014 , GRCh37.p13 chr19: 10,652,158-10,653,690 ATG4D
    nsv5590135copy number variation1nstd207human GRCh38 chr19: 10,547,725-10,548,058 , GRCh37.p13 chr19: 10,658,401-10,658,734 ATG4D
    nsv5526162copy number variation1nstd206human GRCh38 chr19: 10,547,705-10,548,079 , GRCh37.p13 chr19: 10,658,381-10,658,755 ATG4D
    nsv5375305translocation1nstd200human GRCh38 chr19: 10,548,059-10,548,059 , GRCh38 chr19: 10,547,739-10,547,739 , GRCh37.p13 chr19: 10,658,415-10,658,415 , GRCh37.p13 chr19: 10,658,735-10,658,735 ATG4D
    nsv5327274copy number variation1nstd204human GRCh38.p13 chr19: 10,550,920-10,562,660 , GRCh37.p13 chr19: 10,661,596-10,673,336 ATG4D, RNU7-140P, 2 more genes
    nsv5294323copy number variation1nstd204human GRCh38.p13 chr19: 10,550,701-10,562,800 , GRCh37.p13 chr19: 10,661,377-10,673,476 MIR1238, ATG4D, 2 more genes
    nsv5291380copy number variation1nstd204human GRCh38.p13 chr19: 10,335,201-10,670,200 , GRCh37.p13 chr19: 10,445,877-10,780,876 ICAM3, MIR1181, 15 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5285636copy number variation1nstd204human GRCh38.p13 chr19: 10,550,950-10,563,099 , GRCh37.p13 chr19: 10,661,626-10,673,775 ATG4D, RNU7-140P, 2 more genes
    nsv5283750copy number variation1nstd204human GRCh37.p13 chr19: 10,617,077-10,686,476 , GRCh38.p13 chr19: 10,506,401-10,575,800 CDKN2D, AP1M2, 5 more genes
    nsv5208597mobile element deletion1nstd204human GRCh38.p13 chr19: 10,542,243-10,542,553 , GRCh37.p13 chr19: 10,652,919-10,653,229 ATG4D
    nsv4907496mobile element deletion1nstd200human GRCh38 chr19: 10,542,253-10,542,544 , GRCh37.p13 chr19: 10,652,929-10,653,220 ATG4D
    nsv4852994copy number variation1nstd200human GRCh37 chr19: 10,658,413-10,658,736 , GRCh38.p12 chr19: 10,547,737-10,548,060 ATG4D
    nsv4769742mobile element deletion1nstd200human GRCh37 chr19: 10,652,929-10,653,220 , GRCh38.p12 chr19: 10,542,253-10,542,544 ATG4D
    nsv4747606copy number variation1nstd199human GRCh38.p12 chr19: 10,550,740-10,557,138 , GRCh37 chr19: 10,661,416-10,667,814 KRI1, ATG4D, 2 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
    nsv4457721copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286 CDKN2D, QTRT1, 24 more genes
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4266620copy number variation1nstd166human GRCh37.p13 chr19: 10,640,850-10,653,740 , GRCh38.p12 chr19: 10,530,174-10,543,064 ATG4D
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