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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905729copy number variation1nstd209human GRCh38 chr4: 70,840,012-70,840,179 , GRCh37.p13 chr4: 71,705,729-71,705,896 GRSF1
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5891547copy number variation1nstd209human GRCh38 chr4: 70,831,845-70,831,962 , GRCh37.p13 chr4: 71,697,562-71,697,679 GRSF1
    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
    nsv5617532insertion1nstd207human GRCh38 chr4: 70,840,221-70,840,221 , GRCh37.p13 chr4: 71,705,938-71,705,938 GRSF1
    nsv5612237insertion2nstd207human GRCh38 chr4: 70,840,012-70,840,012 , GRCh37.p13 chr4: 71,705,729-71,705,729 GRSF1
    nsv5581693copy number variation1nstd207human GRCh38 chr4: 70,840,012-70,840,116 , GRCh37.p13 chr4: 71,705,729-71,705,833 GRSF1
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5467770copy number variation1nstd206human GRCh38 chr4: 70,812,860-70,814,359 , GRCh37.p13 chr4: 71,678,577-71,680,076 GRSF1
    nsv5216410mobile element deletion1nstd204human GRCh38.p13 chr4: 70,837,273-70,837,588 , GRCh37.p13 chr4: 71,702,990-71,703,305 GRSF1
    nsv5091328mobile element insertion1nstd203human GRCh38 chr4: 70,828,908-70,828,918 , GRCh37.p13 chr4: 71,694,625-71,694,635 GRSF1
    nsv5090926mobile element insertion1nstd203human GRCh38 chr4: 70,821,041-70,821,058 , GRCh37.p13 chr4: 71,686,758-71,686,775 GRSF1
    nsv5089762mobile element insertion1nstd203human GRCh38 chr4: 70,828,912-70,828,918 , GRCh37.p13 chr4: 71,694,629-71,694,635 GRSF1
    nsv5081809mobile element insertion1nstd203human GRCh38 chr4: 70,833,048-70,833,063 , GRCh37.p13 chr4: 71,698,765-71,698,780 GRSF1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925785copy number variation1nstd200human GRCh38 chr4: 70,822,398-70,823,378 , GRCh37.p13 chr4: 71,688,115-71,689,095 GRSF1
    nsv4922880copy number variation1nstd200human GRCh38 chr4: 70,834,227-70,835,375 , GRCh37.p13 chr4: 71,699,944-71,701,092 GRSF1
    nsv4922879copy number variation1nstd200human GRCh38 chr4: 70,826,597-70,827,516 , GRCh37.p13 chr4: 71,692,314-71,693,233 GRSF1
    nsv4922878copy number variation1nstd200human GRCh38 chr4: 70,824,727-70,827,242 , GRCh37.p13 chr4: 71,690,444-71,692,959 GRSF1
    nsv4922877copy number variation1nstd200human GRCh38 chr4: 70,816,124-70,816,255 , GRCh37.p13 chr4: 71,681,841-71,681,972 GRSF1
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