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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941219copy number variation1nstd209human GRCh38 chr14: 34,520,139-34,520,461 , GRCh37.p13 chr14: 34,989,345-34,989,667 EAPP
    nsv5720882mobile element insertion1nstd211human GRCh38 chr14: 34,536,890-34,536,890 , GRCh37.p13 chr14: 35,006,096-35,006,096 EAPP
    nsv5650544insertion1nstd207human GRCh38 chr14: 34,514,903-34,514,903 , GRCh37.p13 chr14: 34,984,109-34,984,109 EAPP
    nsv5536585insertion1nstd206human GRCh38 chr14: 34,514,921-34,514,954 , GRCh37.p13 chr14: 34,984,127-34,984,160 EAPP
    nsv5510593copy number variation1nstd206human GRCh38 chr14: 34,513,713-34,519,713 , GRCh37.p13 chr14: 34,982,919-34,988,919 EAPP
    nsv5507491copy number variation1nstd206human GRCh38 chr14: 34,526,129-34,533,313 , GRCh37.p13 chr14: 34,995,335-35,002,519 EAPP
    nsv5507101copy number variation1nstd206human GRCh38 chr14: 34,520,448-34,521,927 , GRCh37.p13 chr14: 34,989,654-34,991,133 EAPP
    nsv5505778copy number variation1nstd206human GRCh38 chr14: 34,525,975-34,529,091 , GRCh37.p13 chr14: 34,995,181-34,998,297 EAPP
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5497674copy number variation1nstd206human GRCh38 chr14: 34,517,311-34,518,397 , GRCh37.p13 chr14: 34,986,517-34,987,603 EAPP
    nsv5496274copy number variation1nstd206human GRCh38 chr14: 34,527,713-34,541,713 , GRCh37.p13 chr14: 34,996,919-35,010,919 EAPP, LOC105370447, 1 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv5374485translocation1nstd200human GRCh38 chr14: 34,554,721-34,554,721 , GRCh38 chr14: 34,528,490-34,528,490 , GRCh37.p13 chr14: 34,997,696-34,997,696 , GRCh37.p13 chr14: 35,023,927-35,023,927 RNU1-28P, EAPP, 1 more genes
    nsv5357084translocation1nstd200human GRCh38 chr14: 34,530,528-34,530,528 , GRCh38 chr14: 34,530,445-34,530,445 , GRCh37.p13 chr14: 34,999,651-34,999,651 , GRCh37.p13 chr14: 34,999,734-34,999,734 EAPP
    nsv5339943translocation1nstd200human GRCh37 chr14: 35,023,927-35,023,927 , GRCh37 chr14: 34,997,697-34,997,697 , GRCh38.p12 chr14: 34,528,491-34,528,491 , GRCh38.p12 chr14: 34,554,721-34,554,721 RNU1-28P, EAPP, 1 more genes
    nsv5313330copy number variation1nstd204human GRCh37.p13 chr14: 34,998,310-35,023,056 , GRCh38.p13 chr14: 34,529,104-34,553,850 RNU1-27P, EAPP, 3 more genes
    nsv5278779copy number variation1nstd204human GRCh38.p13 chr14: 34,519,601-34,550,800 , GRCh37.p13 chr14: 34,988,807-35,020,006 EAPP, LOC105370449, 3 more genes
    nsv5274793copy number variation1nstd204human GRCh37.p13 chr14: 34,953,507-35,129,206 , GRCh38.p13 chr14: 34,484,301-34,660,000 RNU1-27P, RNU1-28P, 7 more genes
    nsv5272084copy number variation1nstd204human GRCh38.p13 chr14: 34,523,978-34,525,028 , GRCh37.p13 chr14: 34,993,184-34,994,234 EAPP
    nsv5272024copy number variation1nstd204human GRCh38.p13 chr14: 34,514,534-34,516,833 , GRCh37.p13 chr14: 34,983,740-34,986,039 EAPP
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