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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889240copy number variation1nstd209human GRCh38 chr4: 38,479,825-38,850,299 , GRCh37.p13 chr4: 38,481,446-38,851,920 , KLF3, 10 more genes
    nsv5466354copy number variation1nstd206human GRCh38 chr4: 38,797,000-38,828,000 , GRCh37.p13 chr4: 38,798,621-38,829,621 TLR6, TLR1
    nsv5464320copy number variation1nstd206human GRCh38 chr4: 38,809,429-38,862,804 , GRCh37.p13 chr4: 38,811,050-38,864,425 TLR6
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4922528copy number variation1nstd200human GRCh38 chr4: 38,858,204-38,860,909 , GRCh37.p13 chr4: 38,859,825-38,862,530 TLR6
    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
    nsv4588662copy number variation1nstd183human GRCh37 chr4: 38,810,990-38,864,379 , GRCh38.p12 chr4: 38,809,369-38,862,758 TLR6
    nsv4400149copy number variation1nstd174human GRCh37 chr4: 38,810,972-38,864,448 , GRCh38.p12 chr4: 38,809,351-38,862,827 TLR6
    nsv4105557copy number variation1nstd166human GRCh37.p13 chr4: 38,799,000-38,829,500 , GRCh38.p12 chr4: 38,797,379-38,827,879 TLR1, TLR6
    nsv4097714copy number variation1nstd166human GRCh37.p13 chr4: 38,838,707-38,838,773 , GRCh38.p12 chr4: 38,837,086-38,837,152 TLR6
    nsv4092857copy number variation1nstd166human GRCh37.p13 chr4: 38,822,187-38,826,882 , GRCh38.p12 chr4: 38,820,566-38,825,261 TLR6
    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
    nsv3916389copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,447-39,478,764 , GRCh38 chr4: 72,555-39,477,144 , NCBI36 chr4: 62,447-39,155,159 AFAP1-AS1, LINC02481, 540 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
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