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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947939insertion1nstd209human GRCh38 chr3: 9,932,375-9,932,375 , GRCh37.p13 chr3: 9,974,059-9,974,059 IL17RC, CRELD1
    nsv5624425insertion1nstd207human GRCh38 chr3: 9,940,761-9,940,761 , GRCh37.p13 chr3: 9,982,445-9,982,445 CRELD1
    nsv5605183insertion1nstd207human GRCh38 chr3: 9,932,375-9,932,375 , GRCh37.p13 chr3: 9,974,059-9,974,059 CRELD1, IL17RC
    nsv5564436copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,962,155-9,975,297 , GRCh38.p12 chr3: 9,920,471-9,933,613 CRELD1, IL17RC
    nsv5534516insertion1nstd206human GRCh38 chr3: 9,932,375-9,932,375 , GRCh37.p13 chr3: 9,974,059-9,974,059 IL17RC, CRELD1
    nsv5381364copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,976,103-10,191,669 , GRCh38.p12 chr3: 9,934,419-10,149,985 CYCSP10, MARK2P2, 13 more genes
    nsv5311699copy number variation1nstd204human GRCh38.p13 chr3: 9,776,127-10,149,069 , GRCh37.p13 chr3: 9,817,811-10,190,753 EMC3, CYCSP11, 25 more genes
    nsv5207564copy number variation1nstd204human GRCh37.p13 chr3: 9,956,028-10,006,045 , GRCh38.p13 chr3: 9,914,344-9,964,361 EMC3, CRELD1, 5 more genes
    nsv5205129copy number variation1nstd204human GRCh38.p13 chr3: 9,776,301-10,148,700 , GRCh37.p13 chr3: 9,817,985-10,190,384 JAGN1, TTLL3, 25 more genes
    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
    nsv4917719copy number variation1nstd200human GRCh38 chr3: 9,920,913-9,955,071 , GRCh37.p13 chr3: 9,962,597-9,996,755 CRELD1, IL17RC, 2 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796267copy number variation1nstd200human GRCh37 chr3: 9,973,315-9,974,028 , GRCh38.p12 chr3: 9,931,631-9,932,344 CRELD1, IL17RC
    nsv4766381insertion1nstd199human GRCh37 chr3: 9,982,350-9,982,350 , GRCh38.p12 chr3: 9,940,666-9,940,666 CRELD1
    nsv4683755copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,932,387-9,975,297 , GRCh38.p12 chr3: 9,890,703-9,933,613 IL17RC, RNU6-882P, 3 more genes
    nsv4682709copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,743,464-9,986,273 , GRCh38.p12 chr3: 9,701,780-9,944,589 IL17RE, IL17RC, 16 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 LOC105376944, LMCD1, 122 more genes
    nsv4586946copy number variation1nstd183human GRCh37 chr3: 9,974,490-9,974,702 , GRCh38.p12 chr3: 9,932,806-9,933,018 IL17RC, CRELD1
    nsv4578397copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 9,969,850-9,979,790 , GRCh38.p12 chr3: 9,928,166-9,938,106 CRELD1, IL17RC
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