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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894002copy number variation1nstd209human GRCh38 chr3: 9,837,019-9,837,163 , GRCh37.p13 chr3: 9,878,703-9,878,847 RPUSD3
    nsv5582311copy number variation1nstd207human GRCh38 chr3: 9,836,749-9,837,009 , GRCh37.p13 chr3: 9,878,433-9,878,693 TTLL3, RPUSD3, 1 more genes
    nsv5560704sequence alteration1nstd206human GRCh37.p13 chr3: 9,807,275-9,924,747 , GRCh38 chr3: 9,765,591-9,883,063 OGG1, CAMK1, 7 more genes
    nsv5443771copy number variation1nstd206human GRCh38 chr3: 9,837,019-9,837,151 , GRCh37.p13 chr3: 9,878,703-9,878,835 RPUSD3
    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
    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
    nsv4917710copy number variation1nstd200human GRCh38 chr3: 9,840,035-9,846,810 , GRCh37.p13 chr3: 9,881,719-9,888,494 RPUSD3
    nsv4917709copy number variation1nstd200human GRCh38 chr3: 9,833,876-9,836,059 , GRCh37.p13 chr3: 9,875,560-9,877,743 TTLL3, ARPC4-TTLL3, 1 more genes
    nsv4914300copy number variation1nstd200human GRCh38 chr3: 9,495,638-9,874,058 , GRCh37.p13 chr3: 9,537,322-9,915,742 TADA3, CAMK1, 13 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4728197copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,870,413-9,930,906 , GRCh38.p12 chr3: 9,828,729-9,889,222 RPUSD3, CIDEC, 4 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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4451451copy number variation1nstd102humanUncertain significance GRCh37 chr3: 8,883,205-9,954,034 , GRCh38.p12 chr3: 8,841,521-9,912,350 LOC105376949, THUMPD3-AS1, 25 more genes
    nsv4435930copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,453,917-12,015,126 , GRCh38.p12 chr3: 9,412,233-11,973,652 VGLL4, JAGN1, 63 more genes
    nsv4322351inversion1nstd166human GRCh37.p13 chr3: 5,153,487-11,332,347 , GRCh38.p12 chr3: 5,111,802-11,290,661 CAV3, HRH1, 96 more genes
    nsv4090482copy number variation1nstd166human GRCh37.p13 chr3: 9,878,703-9,878,881 , GRCh38.p12 chr3: 9,837,019-9,837,197 RPUSD3
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