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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381431copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,460,738-39,478,735 , GRCh38.p12 chr4: 39,459,118-39,477,115 LIAS, RPL9
    nsv5381430copy number variation2nstd102humanUncertain significance GRCh37 chr4: 39,459,814-39,528,725 , GRCh38.p12 chr4: 39,458,194-39,527,105 LOC401127, LIAS, 3 more genes
    nsv5352817translocation1nstd200human GRCh38 chr4: 39,479,103-39,479,103 , GRCh38 chr4: 39,479,594-39,479,594 , GRCh37.p13 chr4: 39,480,723-39,480,723 , GRCh37.p13 chr4: 39,481,214-39,481,214 LOC401127, LIAS
    nsv5352816translocation1nstd200human GRCh38 chr4: 39,467,283-39,467,283 , GRCh38 chr4: 39,467,345-39,467,345 , GRCh37.p13 chr4: 39,468,965-39,468,965 , GRCh37.p13 chr4: 39,468,903-39,468,903 LIAS
    nsv5199380mobile element insertion1nstd203human GRCh38 chr4: 39,460,177-39,460,191 , GRCh37.p13 chr4: 39,461,797-39,461,811 LIAS
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925512copy number variation1nstd200human GRCh38 chr4: 39,477,476-39,484,244 , GRCh37.p13 chr4: 39,479,096-39,485,864 LIAS, LOC401127
    nsv4925511copy number variation1nstd200human GRCh38 chr4: 39,451,827-39,460,532 , GRCh37.p13 chr4: 39,453,447-39,462,152 RPL9, LIAS, 1 more genes
    nsv4925510copy number variation1nstd200human GRCh38 chr4: 39,424,622-39,574,375 , GRCh37.p13 chr4: 39,426,242-39,575,995 UGDH, SMIM14, 5 more genes
    nsv4809178copy number variation1nstd200human GRCh37 chr4: 39,479,923-39,481,783 , GRCh38.p12 chr4: 39,478,303-39,480,163 LOC401127, LIAS
    nsv4809177copy number variation1nstd200human GRCh37 chr4: 39,479,099-39,485,863 , GRCh38.p12 chr4: 39,477,479-39,484,243 LIAS, LOC401127
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729718copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,116,340-40,293,329 , GRCh38.p12 chr4: 39,114,720-40,291,709 N4BP2, RN7SL558P, 24 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4597270copy number variation1nstd183human GRCh37 chr4: 39,460,318-39,460,509 , GRCh38.p12 chr4: 39,458,698-39,458,889 RPL9, LIAS
    nsv4597269copy number variation1nstd183human GRCh37 chr4: 39,429,122-39,574,155 , GRCh38.p12 chr4: 39,427,502-39,572,535 RPL9, UGDH, 5 more genes
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