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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5686347mobile element insertion1nstd211human GRCh38 chr4: 17,508,730-17,508,730 , GRCh37.p13 chr4: 17,510,353-17,510,353 QDPR
    nsv5676938mobile element insertion1nstd211human GRCh38 chr4: 17,505,818-17,505,818 , GRCh37.p13 chr4: 17,507,441-17,507,441 QDPR
    nsv5438111copy number variation1nstd206human GRCh38 chr4: 17,507,716-17,508,237 , GRCh37.p13 chr4: 17,509,339-17,509,860 QDPR
    nsv5402180mobile element insertion1nstd206human GRCh38 chr4: 17,505,818-17,505,869 , GRCh37.p13 chr4: 17,507,441-17,507,492 QDPR
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925333copy number variation1nstd200human GRCh38 chr4: 16,822,715-17,819,702 , GRCh37.p13 chr4: 16,824,338-17,821,325 LDB2, LINC02493, 14 more genes
    nsv4921736copy number variation1nstd200human GRCh38 chr4: 17,502,280-17,505,634 , GRCh37.p13 chr4: 17,503,903-17,507,257 QDPR
    nsv4921735copy number variation1nstd200human GRCh38 chr4: 17,484,311-17,486,741 , GRCh37.p13 chr4: 17,485,934-17,488,364 QDPR
    nsv4809066copy number variation1nstd200human GRCh37 chr4: 16,824,339-17,821,325 , GRCh38.p12 chr4: 16,822,716-17,819,702 LOC105374507, CLRN2, 14 more genes
    nsv4799599copy number variation1nstd200human GRCh37 chr4: 17,507,073-17,507,914 , GRCh38.p12 chr4: 17,505,450-17,506,291 QDPR
    nsv4799598copy number variation1nstd200human GRCh37 chr4: 17,503,903-17,507,257 , GRCh38.p12 chr4: 17,502,280-17,505,634 QDPR
    nsv4799597copy number variation1nstd200human GRCh37 chr4: 17,485,934-17,488,364 , GRCh38.p12 chr4: 17,484,311-17,486,741 QDPR
    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
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