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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673485copy number variation1nstd102humanPathogenic GRCh37 chr3: 53,125,899-53,226,302 , GRCh38.p12 chr3: 53,091,883-53,192,286 PRKCD, RFT1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5434110copy number variation1nstd206human GRCh38 chr3: 53,184,234-53,214,344 , GRCh37.p13 chr3|NW_004775426.1: 33,189-63,299 , GRCh37.p13 chr3: 53,218,250-53,248,360 PRKCD
    nsv5381422copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,125,899-53,215,768 , GRCh38.p12 chr3: 53,091,883-53,181,752 RFT1, PRKCD
    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
    nsv4914353copy number variation1nstd200human GRCh38 chr3: 53,113,856-53,320,010 , GRCh37.p13 chr3|NW_004775426.1: 1-168,965 , GRCh37.p13 chr3: 53,185,062-53,354,037 TKT, PRKCD, 3 more genes
    nsv4914351copy number variation1nstd200human GRCh38 chr3: 53,061,850-53,588,762 , GRCh37.p13 chr3|NW_004775426.1: 1-263,861 , GRCh37.p13 chr3: 53,095,866-53,622,789 RFT1, TKT, 8 more genes
    nsv4911405copy number variation1nstd200human GRCh38 chr3: 53,171,247-53,174,816 , GRCh37.p13 chr3|NW_004775426.1: 20,202-23,771 , GRCh37.p13 chr3: 53,205,263-53,208,832 PRKCD
    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
    nsv4793993copy number variation1nstd200human GRCh37 chr3: 53,147,872-53,354,037 , GRCh38.p12 chr3: 53,113,856-53,320,010 PRKCD, DCP1A, 3 more genes
    nsv4596525copy number variation1nstd183human GRCh37 chr3: 53,195,079-53,195,660 , GRCh38.p12 chr3: 53,161,063-53,161,644 PRKCD
    nsv4572220mobile element insertion1nstd166human GRCh37.p13 chr3: 53,194,989-53,194,989 , GRCh38.p12 chr3: 53,160,973-53,160,973 PRKCD
    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
    nsv4087766copy number variation1nstd166human GRCh37.p13 chr3: 53,200,166-53,206,889 , GRCh38.p12 chr3: 53,166,150-53,172,873 PRKCD
    nsv4076459copy number variation1nstd166human GRCh37.p13 chr3: 53,196,156-53,198,093 , GRCh38.p12 chr3: 53,162,140-53,164,077 PRKCD
    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
    nsv3959761insertion1nstd168human GRCh38 chr3: 53,179,887-53,201,095 , GRCh37.p13 chr3|NW_004775426.1: 28,842-50,050 , GRCh37.p13 chr3: 53,213,903-53,235,111 PRKCD
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