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Items: 1 to 20 of 498

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948331insertion1nstd209human GRCh38 chr4: 119,499,965-119,499,965 , GRCh37.p13 chr4: 120,421,120-120,421,120 PDE5A, SEPTIN7P14
    nsv5900328copy number variation1nstd209human GRCh38 chr4: 119,575,466-119,577,214 , GRCh37.p13 chr4: 120,496,621-120,498,369 PDE5A
    nsv5894402copy number variation1nstd209human GRCh38 chr4: 119,597,650-119,603,009 , GRCh37.p13 chr4: 120,518,805-120,524,164 PDE5A
    nsv5890836copy number variation1nstd209human GRCh38 chr4: 119,627,783-119,627,848 , GRCh37.p13 chr4: 120,548,938-120,549,003 LOC107986192, PDE5A
    nsv5837865copy number variation1nstd209human GRCh38 chr4: 119,600,471-119,603,070 , GRCh37.p13 chr4: 120,521,626-120,524,225 PDE5A
    nsv5837864copy number variation1nstd209human GRCh38 chr4: 119,575,316-119,576,791 , GRCh37.p13 chr4: 120,496,471-120,497,946 PDE5A
    nsv5837637copy number variation1nstd209human GRCh38 chr4: 119,597,534-119,602,770 , GRCh37.p13 chr4: 120,518,689-120,523,925 PDE5A
    nsv5837636copy number variation1nstd209human GRCh38 chr4: 119,575,442-119,577,195 , GRCh37.p13 chr4: 120,496,597-120,498,350 PDE5A
    nsv5724556mobile element insertion1nstd211human GRCh38 chr4: 119,505,833-119,505,833 , GRCh37.p13 chr4: 120,426,988-120,426,988 PDE5A
    nsv5720333mobile element insertion2nstd211human GRCh38 chr4: 119,562,420-119,562,420 , GRCh37.p13 chr4: 120,483,575-120,483,575 PDE5A
    nsv5685935mobile element insertion2nstd211human GRCh38 chr4: 119,540,198-119,540,198 , GRCh37.p13 chr4: 120,461,353-120,461,353 PDE5A
    nsv5681937mobile element insertion1nstd211human GRCh38 chr4: 119,568,754-119,568,754 , GRCh37.p13 chr4: 120,489,909-120,489,909 PDE5A
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5559537mobile element insertion1nstd206human GRCh38 chr4: 119,562,420-119,562,471 , GRCh37.p13 chr4: 120,483,575-120,483,626 PDE5A
    nsv5559076mobile element insertion1nstd206human GRCh38 chr4: 119,505,833-119,505,884 , GRCh37.p13 chr4: 120,426,988-120,427,039 PDE5A
    nsv5540620insertion1nstd206human GRCh38 chr4: 119,527,767-119,527,818 , GRCh37.p13 chr4: 120,448,922-120,448,973 PDE5A
    nsv5469072copy number variation1nstd206human GRCh38 chr4: 119,504,058-119,773,540 , GRCh37.p13 chr4: 120,425,213-120,694,695 , PDE5A, 2 more genes
    nsv5454009copy number variation1nstd206human GRCh38 chr4: 119,617,947-119,619,007 , GRCh37.p13 chr4: 120,539,102-120,540,162 PDE5A
    nsv5398511mobile element insertion1nstd206human GRCh38 chr4: 119,568,754-119,568,805 , GRCh37.p13 chr4: 120,489,909-120,489,960 PDE5A
    nsv5394194mobile element insertion1nstd206human GRCh38 chr4: 119,540,198-119,540,220 , GRCh37.p13 chr4: 120,461,353-120,461,375 PDE5A
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