U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 299

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131327mobile element insertion1nstd186human GRCh37 chr18: 47,337,315-47,337,366 , GRCh38.p12 chr18: 49,810,945-49,810,996 ACAA2
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970864insertion1nstd209human GRCh38 chr18: 49,810,930-49,810,930 , GRCh37.p13 chr18: 47,337,300-47,337,300 ACAA2
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5935691copy number variation1nstd209human GRCh38 chr18: 49,799,623-49,799,693 , GRCh37.p13 chr18: 47,325,993-47,326,063 ACAA2
    nsv5719700mobile element insertion2nstd211human GRCh38 chr18: 49,810,945-49,810,945 , GRCh37.p13 chr18: 47,337,315-47,337,315 ACAA2
    nsv5698350mobile element insertion2nstd211human GRCh38 chr18: 49,796,731-49,796,731 , GRCh37.p13 chr18: 47,323,101-47,323,101 ACAA2
    nsv5648220insertion1nstd207human GRCh38 chr18: 49,810,930-49,810,930 , GRCh37.p13 chr18: 47,337,300-47,337,300 ACAA2
    nsv5555533mobile element insertion1nstd206human GRCh38 chr18: 49,810,945-49,810,996 , GRCh37.p13 chr18: 47,337,315-47,337,366 ACAA2
    nsv5528668copy number variation1nstd206human GRCh38 chr18: 49,791,094-49,791,276 , GRCh37.p13 chr18: 47,317,464-47,317,646 ACAA2
    nsv5520631copy number variation1nstd206human GRCh38 chr18: 49,799,627-49,799,694 , GRCh37.p13 chr18: 47,325,997-47,326,064 ACAA2
    nsv5418179mobile element insertion1nstd206human GRCh38 chr18: 49,796,731-49,796,782 , GRCh37.p13 chr18: 47,323,101-47,323,152 ACAA2
    nsv5202813mobile element deletion1nstd204human GRCh38.p13 chr18: 49,789,696-49,789,972 , GRCh37.p13 chr18: 47,316,066-47,316,342 ACAA2
    nsv5197800mobile element insertion1nstd203human GRCh38 chr18: 49,810,938-49,810,945 , GRCh37.p13 chr18: 47,337,308-47,337,315 ACAA2
    nsv5197201mobile element insertion1nstd203human GRCh38 chr18: 49,810,935-49,810,944 , GRCh37.p13 chr18: 47,337,305-47,337,314 ACAA2
    nsv5196512mobile element insertion1nstd203human GRCh38 chr18: 49,810,933-49,810,944 , GRCh37.p13 chr18: 47,337,303-47,337,314 ACAA2
    nsv5195903mobile element insertion1nstd203human GRCh38 chr18: 49,810,934-49,810,945 , GRCh37.p13 chr18: 47,337,304-47,337,315 ACAA2
    nsv5193793mobile element insertion1nstd203human GRCh38 chr18: 49,810,929-49,810,945 , GRCh37.p13 chr18: 47,337,299-47,337,315 ACAA2
    nsv5193369mobile element insertion1nstd203human GRCh38 chr18: 49,810,937-49,810,945 , GRCh37.p13 chr18: 47,337,307-47,337,315 ACAA2
    nsv5191020mobile element insertion1nstd203human GRCh38 chr18: 49,810,885-49,810,930 , GRCh37.p13 chr18: 47,337,255-47,337,300 ACAA2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center