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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5443868copy number variation1nstd206human GRCh38 chr3: 53,866,344-53,866,401 , GRCh37.p13 chr3: 53,900,371-53,900,428 ACTR8, IL17RB
    nsv5437944copy number variation1nstd206human GRCh38 chr3: 53,847,380-53,852,848 , GRCh37.p13 chr3: 53,881,407-53,886,875 IL17RB
    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
    nsv4914360copy number variation1nstd200human GRCh38 chr3: 53,823,983-53,901,629 , GRCh37.p13 chr3: 53,858,010-53,935,656 CHDH, SELENOK, 2 more genes
    nsv4914359copy number variation1nstd200human GRCh38 chr3: 53,638,517-54,280,329 , GRCh37.p13 chr3: 53,672,544-54,314,356 ACTR8, CABYRP1, 6 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
    nsv4793995copy number variation1nstd200human GRCh37 chr3: 53,672,544-54,314,356 , GRCh38.p12 chr3: 53,638,517-54,280,329 CHDH, CABYRP1, 6 more genes
    nsv4596526copy number variation1nstd183human GRCh37 chr3: 53,899,450-53,902,041 , GRCh38.p12 chr3: 53,865,423-53,868,014 ACTR8, IL17RB
    nsv4588781copy number variation1nstd183human GRCh37 chr3: 53,865,433-53,934,793 , GRCh38.p12 chr3: 53,831,406-53,900,766 IL17RB, SELENOK, 2 more genes
    nsv4588778copy number variation1nstd183human GRCh37 chr3: 53,405,646-54,428,109 , GRCh38.p12 chr3: 53,371,619-54,394,082 SELENOK, CHDH, 8 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
    nsv4450136copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,413,246-53,955,646 , GRCh38.p12 chr3: 53,379,219-53,921,619 ACTR8, RPS25P4, 4 more genes
    nsv4411482copy number variation1nstd174human GRCh37 chr3: 53,694,418-53,934,781 , GRCh38.p12 chr3: 53,660,391-53,900,754 CACNA1D, CHDH, 3 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
    nsv4089273copy number variation1nstd166human GRCh37.p13 chr3: 53,881,407-53,886,875 , GRCh38.p12 chr3: 53,847,380-53,852,848 IL17RB
    nsv4078102copy number variation1nstd166human GRCh37.p13 chr3: 53,883,421-53,926,003 , GRCh38.p12 chr3: 53,849,394-53,891,976 IL17RB, ACTR8, 1 more genes
    nsv4074688copy number variation1nstd166human GRCh37.p13 chr3: 53,081,392-54,249,627 , GRCh38.p12 chr3: 53,047,376-54,215,600 SELENOK, PRKCD, 15 more genes
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