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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903215copy number variation1nstd209human GRCh38 chr3: 47,430,153-47,533,200 , GRCh37.p13 chr3: 47,471,643-47,574,690 BOLA2P2, LOC105377073, 3 more genes
    nsv5890764copy number variation1nstd209human GRCh38 chr3: 47,497,417-47,497,479 , GRCh37.p13 chr3: 47,538,907-47,538,969 ELP6
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5836337copy number variation2nstd209human GRCh38 chr3: 47,489,762-47,503,501 , GRCh37.p13 chr3: 47,531,252-47,544,991 ELP6, BOLA2P2
    nsv5836029copy number variation2nstd209human GRCh38 chr3: 47,514,101-47,518,808 , GRCh37.p13 chr3: 47,555,591-47,560,298 ELP6
    nsv5678645mobile element insertion1nstd211human GRCh38 chr3: 47,507,948-47,507,948 , GRCh37.p13 chr3: 47,549,438-47,549,438 ELP6
    nsv5567483copy number variation1nstd207human GRCh38 chr3: 47,497,417-47,497,479 , GRCh37.p13 chr3: 47,538,907-47,538,969 ELP6
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5450889copy number variation1nstd206human GRCh38 chr3: 47,485,433-47,529,811 , GRCh37.p13 chr3: 47,526,923-47,571,301 BOLA2P2, ELP6
    nsv5448661copy number variation1nstd206human GRCh38 chr3: 47,504,715-47,507,089 , GRCh37.p13 chr3: 47,546,205-47,548,579 ELP6
    nsv5441556copy number variation1nstd206human GRCh38 chr3: 47,497,419-47,497,480 , GRCh37.p13 chr3: 47,538,909-47,538,970 ELP6
    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
    nsv4924397copy number variation1nstd200human GRCh38 chr3: 47,344,940-47,923,420 , GRCh37.p13 chr3: 47,386,430-47,964,910 PTPN23, DHX30, 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
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4793964copy number variation1nstd200human GRCh37 chr3: 47,471,581-47,574,737 , GRCh38.p12 chr3: 47,430,091-47,533,247 ELP6, LOC105377073, 3 more genes
    nsv4588742copy number variation1nstd183human GRCh37 chr3: 47,548,985-47,594,981 , GRCh38.p12 chr3: 47,507,495-47,553,491 ELP6, LOC105377074
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
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