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Items: 1 to 20 of 386

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7144672insertion1nstd232human GRCh37.p13 chr8: 124,346,563-124,346,563 , GRCh38.p12 chr8: 123,334,323-123,334,323 ATAD2
    nsv7143905insertion1nstd232human GRCh37.p13 chr8: 124,381,414-124,381,414 , GRCh38.p12 chr8: 123,369,174-123,369,174 ATAD2
    nsv7142325insertion1nstd232human GRCh37.p13 chr8: 124,346,261-124,346,261 , GRCh38.p12 chr8: 123,334,021-123,334,021 ATAD2
    nsv7140268insertion1nstd232human GRCh37.p13 chr8: 124,346,564-124,346,564 , GRCh38.p12 chr8: 123,334,324-123,334,324 ATAD2
    nsv7137260insertion1nstd232human GRCh37.p13 chr8: 124,340,820-124,340,820 , GRCh38.p12 chr8: 123,328,580-123,328,580 ATAD2
    nsv7077052inversion1nstd229human GRCh38 chr8: 122,556,885-123,611,669 , GRCh37.p13 chr8: 123,569,124-124,623,909 RNY4P5, ZHX2, 27 more genes
    nsv7064991inversion1nstd229human GRCh38 chr8: 122,266,535-123,404,204 , GRCh37.p13 chr8: 123,278,774-124,416,444 FAM83A, LOC107986904, 26 more genes
    nsv7062653inversion1nstd229human GRCh38 chr8: 123,244,106-123,396,623 , GRCh37.p13 chr8: 124,256,346-124,408,863 RNU6-628P, MIR548AA1, 8 more genes
    nsv7060368inversion1nstd229human GRCh38 chr8: 123,324,118-123,324,156 , GRCh37.p13 chr8: 124,336,358-124,336,396 ATAD2
    nsv6853740copy number variation1nstd229human GRCh38 chr8: 123,365,520-123,365,714 , GRCh37.p13 chr8: 124,377,760-124,377,954 ATAD2
    nsv6851014copy number variation1nstd229human GRCh38 chr8: 123,396,423-123,396,473 , GRCh37.p13 chr8: 124,408,663-124,408,713 ATAD2
    nsv6839654copy number variation1nstd229human GRCh38 chr8: 123,324,701-123,368,600 , GRCh37.p13 chr8: 124,336,941-124,380,840 MIR548D1, DUTP2, 3 more genes
    nsv6839106copy number variation1nstd229human GRCh38 chr8: 123,352,151-123,352,275 , GRCh37.p13 chr8: 124,364,391-124,364,515 DUTP2, ATAD2
    nsv6838990copy number variation1nstd229human GRCh38 chr8: 123,382,491-123,387,719 , GRCh37.p13 chr8: 124,394,731-124,399,959 ATAD2
    nsv6838955copy number variation1nstd229human GRCh38 chr8: 123,259,256-123,380,191 , GRCh37.p13 chr8: 124,271,496-124,392,431 ZHX1-C8orf76, ZHX1, 7 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6569805inversion1nstd223human GRCh38 chr8: 123,372,912-123,373,790 , GRCh37.p13 chr8: 124,385,152-124,386,030 ATAD2
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