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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971585insertion1nstd209human GRCh38 chr14: 35,107,587-35,107,587 , GRCh37.p13 chr14: 35,576,793-35,576,793 PPP2R3C, LOC101927178
    nsv5930047copy number variation1nstd209human GRCh38 chr14: 35,042,551-35,131,102 , GRCh37.p13 chr14: 35,511,757-35,600,308 PRORP, PPP2R3C, 2 more genes
    nsv5866434copy number variation1nstd209human GRCh38 chr14: 35,100,620-35,103,419 , GRCh37.p13 chr14: 35,569,826-35,572,625 LOC101927178, PPP2R3C
    nsv5866286copy number variation1nstd209human GRCh38 chr14: 35,096,020-35,103,419 , GRCh37.p13 chr14: 35,565,226-35,572,625 PPP2R3C, LOC101927178
    nsv5865070copy number variation1nstd209human GRCh38 chr14: 35,092,218-35,093,517 , GRCh37.p13 chr14: 35,561,424-35,562,723 LOC101927178, PPP2R3C
    nsv5863235copy number variation1nstd209human GRCh38 chr14: 35,087,768-35,089,967 , GRCh37.p13 chr14: 35,556,974-35,559,173 PPP2R3C, LOC101927178
    nsv5863139copy number variation2nstd209human GRCh38 chr14: 35,081,589-35,083,817 , GRCh37.p13 chr14: 35,550,795-35,553,023 PPP2R3C, LOC101927178, 1 more genes
    nsv5860796copy number variation1nstd209human GRCh38 chr14: 35,096,021-35,098,319 , GRCh37.p13 chr14: 35,565,227-35,567,525 LOC101927178, PPP2R3C
    nsv5852143copy number variation1nstd209human GRCh38 chr14: 35,090,518-35,091,717 , GRCh37.p13 chr14: 35,559,724-35,560,923 LOC101927178, PPP2R3C
    nsv5718573mobile element insertion1nstd211human GRCh38 chr14: 35,106,297-35,106,297 , GRCh37.p13 chr14: 35,575,503-35,575,503 PPP2R3C, LOC101927178
    nsv5707374mobile element insertion2nstd211human GRCh38 chr14: 35,094,645-35,094,645 , GRCh37.p13 chr14: 35,563,851-35,563,851 LOC101927178, PPP2R3C
    nsv5547356insertion1nstd206human GRCh38 chr14: 35,107,607-35,107,638 , GRCh37.p13 chr14: 35,576,813-35,576,844 LOC101927178, PPP2R3C
    nsv5511997copy number variation1nstd206human GRCh38 chr14: 35,120,018-35,120,445 , GRCh37.p13 chr14: 35,589,224-35,589,651 PRORP, PPP2R3C
    nsv5498213copy number variation1nstd206human GRCh38 chr14: 35,090,376-35,090,441 , GRCh37.p13 chr14: 35,559,582-35,559,647 LOC101927178, PPP2R3C
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5493990copy number variation1nstd206human GRCh38 chr14: 35,089,787-35,090,932 , GRCh37.p13 chr14: 35,558,993-35,560,138 PPP2R3C, LOC101927178
    nsv5429218mobile element insertion1nstd206human GRCh38 chr14: 35,094,645-35,094,696 , GRCh37.p13 chr14: 35,563,851-35,563,902 PPP2R3C, LOC101927178
    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
    nsv5159320mobile element insertion1nstd203human GRCh38 chr14: 35,094,208-35,094,208 , GRCh37.p13 chr14: 35,563,414-35,563,414 PPP2R3C, LOC101927178
    nsv5156992mobile element insertion1nstd203human GRCh38 chr14: 35,092,370-35,092,379 , GRCh37.p13 chr14: 35,561,576-35,561,585 PPP2R3C, LOC101927178
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