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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
    nsv5438903copy number variation1nstd206human GRCh38 chr4: 9,664,808-10,441,581 , GRCh37.p13 chr4: 9,666,432-10,443,205 , RNA5SP154, 19 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925271copy number variation1nstd200human GRCh38 chr4: 9,965,169-10,656,724 , GRCh37.p13 chr4: 9,966,793-10,658,348 , LOC100129344, 17 more genes
    nsv4925262copy number variation1nstd200human GRCh38 chr4: 9,666,725-10,576,182 , GRCh37.p13 chr4: 9,668,349-10,577,806 , OR7E35P, 23 more genes
    nsv4925243copy number variation1nstd200human GRCh38 chr4: 8,427,161-10,250,688 , GRCh37.p13 chr4: 8,428,888-10,252,312 , OR7E35P, 68 more genes
    nsv4805256copy number variation1nstd200human GRCh37 chr4: 9,966,793-10,658,348 , GRCh38.p12 chr4: 9,965,169-10,656,724 , LOC105374482, 17 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
    nsv4729702copy number variation1nstd102humanUncertain significance GRCh37 chr4: 9,748,015-10,942,200 , GRCh38.p12 chr4: 9,746,391-10,940,576 OR7E35P, LOC100130072, 21 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
    nsv4684136copy number variation1nstd102humanUncertain significance GRCh37 chr4: 9,896,293-13,242,797 , GRCh38.p12 chr4: 9,894,669-13,241,173 LOC105374492, LOC105374489, 35 more genes
    nsv4674692copy number variation1nstd102humanLikely benign GRCh37 chr4: 9,544,188-10,738,030 , GRCh38.p12 chr4: 9,542,568-10,736,406 RNA5SP154, LOC105374481, 28 more genes
    nsv4674435copy number variation1nstd102humanLikely benign GRCh37 chr4: 9,501,650-10,794,722 , GRCh38.p12 chr4: 9,500,006-10,793,098 RPS3AP19, LOC100422637, 31 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
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