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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120903copy number variation1nstd186human GRCh37 chr14: 50,118,887-50,119,027 , GRCh38.p12 chr14: 49,652,169-49,652,309 POLE2
    nsv5944085copy number variation1nstd209human GRCh38 chr14: 49,652,152-49,652,308 , GRCh37.p13 chr14: 50,118,870-50,119,026 POLE2
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5932579copy number variation1nstd209human GRCh38 chr14: 49,682,987-49,683,441 , GRCh37.p13 chr14: 50,149,705-50,150,159 POLE2, RNU6ATAC30P
    nsv5852584copy number variation1nstd209human GRCh38 chr14: 49,659,270-49,660,269 , GRCh37.p13 chr14: 50,125,988-50,126,987 POLE2
    nsv5721607mobile element insertion2nstd211human GRCh38 chr14: 49,653,661-49,653,661 , GRCh37.p13 chr14: 50,120,379-50,120,379 POLE2
    nsv5711203mobile element insertion1nstd211human GRCh38 chr14: 49,669,617-49,669,617 , GRCh37.p13 chr14: 50,136,335-50,136,335 POLE2
    nsv5602928copy number variation1nstd207human GRCh38 chr14: 49,652,152-49,652,308 , GRCh37.p13 chr14: 50,118,870-50,119,026 POLE2
    nsv5536477insertion1nstd206human GRCh38 chr14: 49,682,987-49,682,987 , GRCh37.p13 chr14: 50,149,705-50,149,705 RNU6ATAC30P, POLE2
    nsv5513296copy number variation1nstd206human GRCh38 chr14: 49,652,169-49,652,309 , GRCh37.p13 chr14: 50,118,887-50,119,027 POLE2
    nsv5507511copy number variation1nstd206human GRCh38 chr14: 49,682,506-49,684,845 , GRCh37.p13 chr14: 50,149,224-50,151,563 POLE2, RNU6ATAC30P
    nsv5505832copy number variation1nstd206human GRCh38 chr14: 49,644,294-49,729,211 , GRCh37.p13 chr14: 50,111,012-50,195,929 KLHDC1, RNU6ATAC30P, 2 more genes
    nsv5414159mobile element insertion1nstd206human GRCh38 chr14: 49,669,617-49,669,668 , GRCh37.p13 chr14: 50,136,335-50,136,386 POLE2
    nsv5384513mobile element deletion1nstd186human GRCh37 chr14: 50,118,887-50,119,027 , GRCh38.p12 chr14: 49,652,169-49,652,309 POLE2
    nsv5369243translocation1nstd200human GRCh38 chr14: 49,661,799-49,661,799 , GRCh38 chr6: 14,576,222-14,576,222 , GRCh37.p13 chr6: 14,576,453-14,576,453 , GRCh37.p13 chr14: 50,128,517-50,128,517 LOC101928354, POLE2
    nsv5357223translocation1nstd200human GRCh38 chr14: 49,683,447-49,683,447 , GRCh38 chr14: 49,682,987-49,682,987 , GRCh37.p13 chr14: 50,149,705-50,149,705 , GRCh37.p13 chr14: 50,150,165-50,150,165 RNU6ATAC30P, POLE2
    nsv5340340translocation1nstd200human GRCh37 chr6: 14,576,453-14,576,453 , GRCh37 chr14: 50,128,517-50,128,517 , GRCh38.p12 chr14: 49,661,799-49,661,799 , GRCh38.p12 chr6: 14,576,222-14,576,222 POLE2, LOC101928354
    nsv5332769translocation1nstd200human GRCh37 chr14: 50,119,027-50,119,027 , GRCh37 chr14: 50,118,887-50,118,887 , GRCh38.p12 chr14: 49,652,309-49,652,309 , GRCh38.p12 chr14: 49,652,169-49,652,169 POLE2
    nsv5331972translocation1nstd200human GRCh37 chr14: 50,150,165-50,150,165 , GRCh37 chr14: 50,149,705-50,149,705 , GRCh38.p12 chr14: 49,683,447-49,683,447 , GRCh38.p12 chr14: 49,682,987-49,682,987 RNU6ATAC30P, POLE2
    nsv5303523copy number variation1nstd204human GRCh38.p13 chr14: 49,649,443-49,650,012 , GRCh37.p13 chr14: 50,116,161-50,116,730 POLE2
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