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Items: 1 to 20 of 128

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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
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 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
    nsv4729663copy number variation1nstd102humanUncertain significance GRCh37 chr4: 20,286,376-21,087,147 , GRCh38.p12 chr4: 20,284,753-21,085,524 PACRGL, LOC105374515, 4 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
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 USP17L30, LOC100422637, 394 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
    nsv4578568copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,529,798-22,750,583 , GRCh38.p12 chr4: 13,528,174-22,748,960 RPL21P46, LOC107986187, 88 more genes
    nsv4347791copy number variation1nstd102humanPathogenic GRCh37 chr4: 19,186,845-24,548,281 , GRCh38.p12 chr4: 19,185,222-24,546,658 PACRGL, LOC105374528, 29 more genes
    nsv4347528copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519 MTCO3P44, LINC01097, 148 more genes
    nsv4104760copy number variation1nstd166human GRCh37.p13 chr4: 20,369,645-20,420,781 , GRCh38.p12 chr4: 20,368,022-20,419,158 SLIT2-IT1, SLIT2
    nsv4100825copy number variation1nstd166human GRCh37.p13 chr4: 20,285,553-21,087,145 , GRCh38.p12 chr4: 20,283,930-21,085,522 SLIT2, KCNIP4, 4 more genes
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 OR7E99P, FBXL5, 446 more genes
    nsv3923187copy number variation1nstd102humanUncertain significance NCBI36 chr4: 16,652,102-22,135,636 , GRCh38 chr4: 17,041,381-22,524,915 , GRCh37 chr4: 17,043,004-22,526,538 QDPR, MTND5P4, 38 more genes
    nsv3920814copy number variation1nstd102humanUncertain significance GRCh37 chr4: 19,188,467-20,840,094 , NCBI36 chr4: 18,797,565-20,449,192 , GRCh38 chr4: 19,186,844-20,838,471 SLIT2, KCNIP4, 9 more genes
    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
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