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Items: 1 to 20 of 197

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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
    nsv5892691copy number variation1nstd209human GRCh38 chr4: 70,246,493-70,246,588 , GRCh37.p13 chr4: 71,112,210-71,112,305 CSN3
    nsv5890114copy number variation1nstd209human GRCh38 chr4: 70,242,280-70,242,473 , GRCh37.p13 chr4: 71,107,997-71,108,190 CSN3
    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
    nsv5566833copy number variation1nstd207human GRCh38 chr4: 70,242,280-70,242,473 , GRCh37.p13 chr4: 71,107,997-71,108,190 CSN3
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5464923copy number variation1nstd206human GRCh38 chr4: 70,242,276-70,242,478 , GRCh37.p13 chr4: 71,107,993-71,108,195 CSN3
    nsv5459643copy number variation1nstd206human GRCh38 chr4: 70,238,366-70,238,936 , GRCh37.p13 chr4: 71,104,083-71,104,653 CSN3
    nsv5387780copy number variation2nstd186human GRCh37 chr4: 71,107,993-71,108,195 , GRCh38.p12 chr4: 70,242,276-70,242,478 CSN3
    nsv5320265copy number variation1nstd204human GRCh38.p13 chr4: 70,242,276-70,242,478 , GRCh37.p13 chr4: 71,107,993-71,108,195 CSN3
    nsv5303781copy number variation1nstd204human GRCh38.p13 chr4: 70,239,837-70,246,033 , GRCh37.p13 chr4: 71,105,554-71,111,750 CSN3
    nsv5229167copy number variation1nstd204human GRCh38.p13 chr4: 70,239,957-70,245,389 , GRCh37.p13 chr4: 71,105,674-71,111,106 CSN3
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925776copy number variation1nstd200human GRCh38 chr4: 70,189,296-70,303,862 , GRCh37.p13 chr4: 71,055,013-71,169,579 FDCSP, CSN3, 1 more genes
    nsv4922861copy number variation1nstd200human GRCh38 chr4: 70,242,276-70,242,478 , GRCh37.p13 chr4: 71,107,993-71,108,195 CSN3
    nsv4922860copy number variation1nstd200human GRCh38 chr4: 70,239,847-70,246,024 , GRCh37.p13 chr4: 71,105,564-71,111,741 CSN3
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800133copy number variation1nstd200human GRCh37 chr4: 71,107,993-71,108,195 , GRCh38.p12 chr4: 70,242,276-70,242,478 CSN3
    nsv4800132copy number variation1nstd200human GRCh37 chr4: 71,105,564-71,111,741 , GRCh38.p12 chr4: 70,239,847-70,246,024 CSN3
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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