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Items: 1 to 20 of 84

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 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
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4559661sequence alteration1nstd166human GRCh37.p13 chr4: 41,747,313-41,747,314 , GRCh38.p12 chr4: 41,745,296-41,745,297 PHOX2B
    nsv3923949copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,498,493-49,581,867 , NCBI36 chr4: 40,193,250-49,276,624 , GRCh38 chr4: 40,496,476-49,579,850 CWH43, LOC100419154, 104 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
    nsv3916848copy number variation1nstd102humanPathogenic GRCh37 chr4: 36,424-47,493,612 , GRCh38 chr4: 36,424-47,491,595 , NCBI36 chr4: 26,424-47,188,369 MIR943, LOC105374340, 634 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 MTND4LP29, RNU6-128P, 2341 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 LOC105377343, PDGFC, 2341 more genes
    nsv3880889copy number variation1nstd102humanPathogenic GRCh37 chr4: 1,356,924-49,659,859 , GRCh38.p12 chr4: 1,363,136-49,657,842 LOC107986262, MTCO3P42, 619 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 LOC112268460, LINC02435, 2345 more genes
    nsv3877750copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-46,339,070 , GRCh38.p12 chr4: 49,556-46,337,053 LOC105369250, HTT-AS, 625 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 LOC100420289, LOC100131038, 2347 more genes
    nsv3876307copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-49,064,044 , GRCh38.p12 chr4: 12,440-49,062,027 ADGRA3, RPS3AP16, 659 more genes
    nsv3875629copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LOC105374433, PCGF3-AS1, 658 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 LOC100422029, H2AZ1, 2358 more genes
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