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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968207inversion1nstd209human GRCh38 chr3: 46,053,712-46,427,427 , GRCh37.p13 chr3: 46,095,204-46,468,918 CCR1, CCR3, 9 more genes
    nsv5563336sequence alteration1nstd206human GRCh38 chr3: 46,053,233-46,427,907 , GRCh37.p13 chr3: 46,094,725-46,469,398 CCR1, UQCRC2P1, 9 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
    nsv4911107copy number variation1nstd200human GRCh38 chr3: 46,205,025-46,206,339 , GRCh37.p13 chr3: 46,246,516-46,247,830 CCR1
    nsv4911106copy number variation1nstd200human GRCh38 chr3: 46,204,968-46,205,539 , GRCh37.p13 chr3: 46,246,459-46,247,030 CCR1
    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
    nsv4790529copy number variation1nstd200human GRCh37 chr3: 46,246,459-46,247,030 , GRCh38.p12 chr3: 46,204,968-46,205,539 CCR1
    nsv4679130copy number variation1nstd189human GRCh37.p13 chr3: 46,211,500-46,354,259 , GRCh38.p12 chr3: 46,170,008-46,312,768 CCR1, CCR3, 2 more genes
    nsv4679026copy number variation1nstd189human GRCh37.p13 chr3: 46,193,305-46,354,259 , GRCh38.p12 chr3: 46,151,813-46,312,768 CCR1, CCR3, 2 more genes
    nsv4567455sequence alteration1nstd166human GRCh37.p13 chr3: 46,094,594-46,469,178 , GRCh38.p12 chr3: 46,053,102-46,427,687 CCR3, XCR1, 9 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
    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
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 RBM5-AS1, PRSS42P, 185 more genes
    nsv3918161copy number variation1nstd102humanUncertain significance NCBI36 chr3: 46,186,825-46,352,571 , GRCh37.p13 chr3: 46,211,821-46,377,567 , GRCh38.p12 chr3: 46,170,329-46,336,076 CCR3, UQCRC2P1, 2 more genes
    nsv3912340copy number variation1nstd102humanLikely benign GRCh37 chr3: 45,733,423-46,319,401 , GRCh38 chr3: 45,691,931-46,277,910 , NCBI36 chr3: 45,708,427-46,294,405 LOC105377063, XCR1, 14 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
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