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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953550insertion1nstd209human GRCh38 chr3: 8,967,240-8,967,240 , GRCh37.p13 chr3: 9,008,924-9,008,924 RAD18
    nsv5728185mobile element insertion2nstd211human GRCh38 chr3: 8,875,657-8,875,657 , GRCh37.p13 chr3: 8,917,341-8,917,341 RAD18
    nsv5551918insertion1nstd206human GRCh38 chr3: 8,937,516-8,937,520 , GRCh37.p13 chr3: 8,979,200-8,979,204 RAD18
    nsv5448612copy number variation1nstd206human GRCh38 chr3: 8,938,375-8,938,561 , GRCh37.p13 chr3: 8,980,059-8,980,245 RAD18
    nsv5438230copy number variation1nstd206human GRCh38 chr3: 8,968,393-8,979,801 , GRCh37.p13 chr3: 9,010,077-9,021,485 SRGAP3, RAD18
    nsv5316250copy number variation1nstd204human GRCh38.p13 chr3: 8,881,953-8,883,438 , GRCh37.p13 chr3: 8,923,637-8,925,122 RAD18
    nsv5209101copy number variation1nstd204human GRCh38.p13 chr3: 8,881,948-8,883,447 , GRCh37.p13 chr3: 8,923,632-8,925,131 RAD18
    nsv5206858copy number variation1nstd204human GRCh38.p13 chr3: 8,882,001-8,883,400 , GRCh37.p13 chr3: 8,923,685-8,925,084 RAD18
    nsv5079741mobile element insertion1nstd203human GRCh38 chr3: 8,892,109-8,892,121 , GRCh37.p13 chr3: 8,933,793-8,933,805 RAD18
    nsv5071257mobile element insertion1nstd203human GRCh38 chr3: 8,955,834-8,955,847 , GRCh37.p13 chr3: 8,997,518-8,997,531 RAD18
    nsv5061868mobile element insertion1nstd203human GRCh38 chr3: 8,943,906-8,943,919 , GRCh37.p13 chr3: 8,985,590-8,985,603 RAD18
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4917673copy number variation1nstd200human GRCh38 chr3: 8,964,646-8,965,295 , GRCh37.p13 chr3: 9,006,330-9,006,979 RAD18
    nsv4917672copy number variation1nstd200human GRCh38 chr3: 8,886,466-8,887,434 , GRCh37.p13 chr3: 8,928,150-8,929,118 RAD18
    nsv4917671copy number variation1nstd200human GRCh38 chr3: 8,867,400-8,878,621 , GRCh37.p13 chr3: 8,909,084-8,920,305 RAD18
    nsv4914297copy number variation1nstd200human GRCh38 chr3: 8,938,347-8,952,326 , GRCh37.p13 chr3: 8,980,031-8,994,010 RAD18
    nsv4914296copy number variation1nstd200human GRCh38 chr3: 8,938,375-8,938,561 , GRCh37.p13 chr3: 8,980,059-8,980,245 RAD18
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796232copy number variation1nstd200human GRCh37 chr3: 9,001,495-9,001,771 , GRCh38.p12 chr3: 8,959,811-8,960,087 RAD18
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