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Items: 1 to 20 of 148

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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
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4921604copy number variation1nstd200human GRCh38 chr4: 13,328,237-13,343,690 , GRCh37.p13 chr4: 13,329,861-13,345,314 HSP90AB2P
    nsv4921600copy number variation1nstd200human GRCh38 chr4: 13,230,135-13,392,033 , GRCh37.p13 chr4: 13,231,759-13,393,657 , HSP90AB2P, 1 more genes
    nsv4799513copy number variation1nstd200human GRCh37 chr4: 13,231,759-13,393,657 , GRCh38.p12 chr4: 13,230,135-13,392,033 , RAB28, 1 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
    nsv4674599copy number variation1nstd102humanUncertain significance GRCh37 chr4: 10,313,041-14,158,188 , GRCh38.p12 chr4: 10,311,417-14,156,564 LINC01085, ZNF518B, 41 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 USP17L30, LOC100422637, 394 more genes
    nsv4674196copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 5,914,109-17,264,668 , GRCh38.p12 chr4: 5,912,382-17,263,045 NKX3-2, BST1, 193 more genes
    nsv4673983copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-27,423,424 , GRCh38.p12 chr4: 68,453-27,421,802 LOC101928306, LINC02261, 439 more genes
    nsv4596870copy number variation1nstd183human GRCh37 chr4: 13,260,705-13,923,604 , GRCh38.p12 chr4: 13,259,081-13,921,980 , LINC01182, 14 more genes
    nsv4589885copy number variation1nstd183human GRCh37 chr4: 13,261,201-13,925,045 , GRCh38.p12 chr4: 13,259,577-13,923,421 , LINC01096, 14 more genes
    nsv4455312copy number variation1nstd102humanPathogenic GRCh37 chr4: 3,374,195-13,468,480 , GRCh38.p12 chr4: 3,372,468-13,466,856 LOC105374358, USP17L12, 198 more genes
    nsv4353435inversion1nstd102humanPathogenic GRCh38 chr4: 8,398,067-17,505,522 , GRCh37.p13 chr4: 8,399,794-17,507,145 NKX3-2, BST1, 152 more genes
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