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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5449129copy number variation1nstd206human GRCh38 chr3: 10,118,957-10,121,332 , GRCh37.p13 chr3: 10,160,641-10,163,016 BRK1
    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
    nsv5381357copy number variation1nstd102humanUncertain significance GRCh37 chr3: 10,103,825-10,184,708 , GRCh38.p12 chr3: 10,062,141-10,143,024 FANCD2, FANCD2OS, 2 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
    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
    nsv5195264mobile element insertion1nstd203human GRCh38 chr3: 10,122,724-10,122,738 , GRCh37.p13 chr3: 10,164,408-10,164,422 BRK1
    nsv5074729mobile element insertion1nstd203human GRCh38 chr3: 10,123,632-10,123,658 , GRCh37.p13 chr3: 10,165,316-10,165,342 BRK1
    nsv5068186mobile element insertion1nstd203human GRCh38 chr3: 10,123,753-10,123,790 , GRCh37.p13 chr3: 10,165,437-10,165,474 BRK1
    nsv5068108mobile element insertion1nstd203human GRCh38 chr3: 10,123,605-10,123,658 , GRCh37.p13 chr3: 10,165,289-10,165,342 BRK1
    nsv5062727mobile element insertion1nstd203human GRCh38 chr3: 10,123,732-10,123,753 , GRCh37.p13 chr3: 10,165,416-10,165,437 BRK1
    nsv5062158mobile element insertion1nstd203human GRCh38 chr3: 10,123,628-10,123,658 , GRCh37.p13 chr3: 10,165,312-10,165,342 BRK1
    nsv5061969mobile element insertion1nstd203human GRCh38 chr3: 10,123,633-10,123,658 , GRCh37.p13 chr3: 10,165,317-10,165,342 BRK1
    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
    nsv4924173copy number variation1nstd200human GRCh38 chr3: 10,123,778-10,125,257 , GRCh37.p13 chr3: 10,165,462-10,166,941 BRK1
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4793841copy number variation1nstd200human GRCh37 chr3: 10,165,462-10,166,941 , GRCh38.p12 chr3: 10,123,778-10,125,257 BRK1
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