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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
    nsv5438135copy number variation1nstd206human GRCh38 chr4: 29,211,940-29,215,046 , GRCh37.p13 chr4: 29,213,562-29,216,668 LINC02472
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4922144copy number variation1nstd200human GRCh38 chr4: 29,209,830-29,247,135 , GRCh37.p13 chr4: 29,211,452-29,248,757 LINC02472
    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
    nsv4729327copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 28,607,146-32,017,466 , GRCh38.p12 chr4: 28,605,524-32,015,844 PCDH7, MESTP3, 20 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
    nsv4588579copy number variation1nstd183human GRCh37 chr4: 29,218,299-29,230,644 , GRCh38.p12 chr4: 29,216,677-29,229,022 LINC02472
    nsv4545224insertion1nstd166human GRCh37.p13 chr4: 29,221,054-29,221,054 , GRCh38.p12 chr4: 29,219,432-29,219,432 LINC02472
    nsv3957837copy number variation1nstd168human GRCh38 chr4: 29,197,740-29,242,905 , GRCh37.p13 chr4: 29,199,362-29,244,527 LINC02472
    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
    nsv3916654copy number variation1nstd102humanPathogenic NCBI36 chr4: 75,040-38,378,382 , GRCh37 chr4: 85,040-38,701,987 , GRCh38 chr4: 85,149-38,700,366 CCKAR, OTOP1, 522 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
    nsv3914239copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,447-33,132,242 , GRCh38 chr4: 72,555-33,130,620 , NCBI36 chr4: 62,447-32,808,637 TMEM271, CC2D2A, 477 more genes
    nsv3911497copy number variation1nstd102humanPathogenic GRCh38 chr4: 16,925,022-32,113,076 , NCBI36 chr4: 16,535,743-31,758,596 , GRCh37 chr4: 16,926,645-32,114,698 LINC02506, LOC105374513, 128 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
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