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Items: 1 to 20 of 324

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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
    nsv5892746copy number variation1nstd209human GRCh38 chr4: 70,754,630-70,754,700 , GRCh37.p13 chr4: 71,620,347-71,620,417 RUFY3
    nsv5686391mobile element insertion1nstd211human GRCh38 chr4: 70,728,032-70,728,032 , GRCh37.p13 chr4: 71,593,749-71,593,749 RUFY3
    nsv5683389mobile element insertion1nstd211human GRCh38 chr4: 70,735,510-70,735,510 , GRCh37.p13 chr4: 71,601,227-71,601,227 RUFY3
    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
    nsv5547789insertion1nstd206human GRCh38 chr4: 70,735,510-70,735,551 , GRCh37.p13 chr4: 71,601,227-71,601,268 RUFY3
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5396681mobile element insertion1nstd206human GRCh38 chr4: 70,728,032-70,728,083 , GRCh37.p13 chr4: 71,593,749-71,593,800 RUFY3
    nsv5094704mobile element insertion1nstd203human GRCh38 chr4: 70,735,500-70,735,510 , GRCh37.p13 chr4: 71,601,217-71,601,227 RUFY3
    nsv5085689mobile element insertion1nstd203human GRCh38 chr4: 70,735,504-70,735,508 , GRCh37.p13 chr4: 71,601,221-71,601,225 RUFY3
    nsv5083378mobile element insertion1nstd203human GRCh38 chr4: 70,735,505-70,735,510 , GRCh37.p13 chr4: 71,601,222-71,601,227 RUFY3
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 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
    nsv4738384copy number variation1nstd199human GRCh37 chr4: 71,598,799-71,598,855 , GRCh38.p12 chr4: 70,733,082-70,733,138 RUFY3
    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
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