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Items: 1 to 20 of 108

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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
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    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
    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
    nsv4588666copy number variation1nstd183human GRCh37 chr4: 39,459,112-39,462,388 , GRCh38.p12 chr4: 39,457,492-39,460,768 RPL9, LIAS
    nsv4588665copy number variation1nstd183human GRCh37 chr4: 39,439,108-39,578,076 , GRCh38.p12 chr4: 39,437,488-39,576,456 RPL9, UGDH, 5 more genes
    nsv4456556copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,423,077-39,573,377 , GRCh38.p12 chr4: 39,421,457-39,571,757 LIAS, RPL9, 5 more genes
    nsv4455245copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,433,497-39,565,064 , GRCh38.p12 chr4: 39,431,877-39,563,444 SMIM14, UGDH, 5 more genes
    nsv3922142copy number variation1nstd102humanUncertain significance GRCh38 chr4: 39,444,586-46,117,146 , NCBI36 chr4: 39,122,601-45,813,920 , GRCh37 chr4: 39,446,206-46,119,163 PGBD3P4, RNU6-1195P, 84 more genes
    nsv3919039copy number variation1nstd102humanBenign NCBI36 chr4: 38,900,123-39,169,625 , GRCh37 chr4: 39,223,728-39,493,230 , GRCh38 chr4: 39,222,108-39,491,610 LIAS, WDR19, 7 more genes
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