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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5895949copy number variation1nstd209human GRCh38 chr3: 9,773,117-9,774,296 , GRCh37.p13 chr3: 9,814,801-9,815,980 OGG1
    nsv5560704sequence alteration1nstd206human GRCh37.p13 chr3: 9,807,275-9,924,747 , GRCh38 chr3: 9,765,591-9,883,063 OGG1, CAMK1, 7 more genes
    nsv5366981translocation1nstd200human GRCh38 chr3: 9,784,075-9,784,075 , GRCh38 chr3: 9,785,116-9,785,116 , GRCh37.p13 chr3: 9,826,800-9,826,800 , GRCh37.p13 chr3: 9,825,759-9,825,759 TADA3, OGG1
    nsv5366980translocation1nstd200human GRCh38 chr3: 9,785,485-9,785,485 , GRCh38 chr3: 9,784,070-9,784,070 , GRCh37.p13 chr3: 9,825,754-9,825,754 , GRCh37.p13 chr3: 9,827,169-9,827,169 TADA3, OGG1
    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
    nsv5218931copy number variation1nstd204human GRCh38.p13 chr3: 9,787,207-9,788,314 , GRCh37.p13 chr3: 9,828,891-9,829,998 TADA3, OGG1
    nsv5212029copy number variation1nstd204human GRCh38.p13 chr3: 9,776,951-9,806,833 , GRCh37.p13 chr3: 9,818,635-9,848,517 ARPC4-TTLL3, TADA3, 2 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
    nsv4917707copy number variation1nstd200human GRCh38 chr3: 9,773,321-9,773,395 , GRCh37.p13 chr3: 9,815,005-9,815,079 OGG1
    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
    nsv4796257copy number variation1nstd200human GRCh37 chr3: 9,814,823-9,815,974 , GRCh38.p12 chr3: 9,773,139-9,774,290 OGG1
    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
    nsv4596712copy number variation1nstd183human GRCh37 chr3: 9,735,597-9,798,140 , GRCh38.p12 chr3: 9,693,913-9,756,456 CAMK1, BRPF1, 3 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
    nsv4472029mobile element insertion1nstd166human GRCh37.p13 chr3: 9,820,201-9,820,201 , GRCh38.p12 chr3: 9,778,517-9,778,517 TADA3, OGG1
    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
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