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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5839480copy number variation1nstd209human GRCh38 chr4: 73,982,086-73,985,847 , GRCh37.p13 chr4: 74,847,803-74,851,564 PPBP, PF4
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5540490insertion1nstd206human GRCh38 chr4: 73,985,711-73,985,761 , GRCh37.p13 chr4: 74,851,428-74,851,478 PPBP
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925806copy number variation1nstd200human GRCh38 chr4: 73,914,317-74,122,469 , GRCh37.p13 chr4: 74,780,034-74,988,186 PPBP, MTHFD2L, 11 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 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
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 SOWAHB, FTLP9, 211 more genes
    nsv4674141copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444 COX18, UGT2B11, 216 more genes
    nsv4557815sequence alteration1nstd166human GRCh38.p12 chr4: 73,839,165-73,995,285 , GRCh37.p13 chr4: 74,704,882-74,861,002 CXCL1, PF4, 7 more genes
    nsv4477004mobile element insertion1nstd166human GRCh37.p13 chr4: 74,852,921-74,852,921 , GRCh38.p12 chr4: 73,987,204-73,987,204 PPBP
    nsv4476761mobile element insertion1nstd166human GRCh37.p13 chr4: 74,851,280-74,851,280 , GRCh38.p12 chr4: 73,985,563-73,985,563 PPBP
    nsv4456913copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,242,784-82,991,431 , GRCh38.p12 chr4: 67,377,066-82,070,278 KPNA2P1, CCNG2, 270 more genes
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