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 246

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911977copy number variation1nstd209human GRCh38 chr11: 102,601,115-102,601,430 , GRCh37.p13 chr11: 102,471,846-102,472,161 MMP20
    nsv5909520copy number variation1nstd209human GRCh38 chr11: 102,591,739-102,593,851 , GRCh37.p13 chr11: 102,462,470-102,464,582 MMP20
    nsv5867303copy number variation2nstd209human GRCh38 chr11: 102,591,696-102,593,895 , GRCh37.p13 chr11: 102,462,427-102,464,626 MMP20
    nsv5707694mobile element insertion2nstd211human GRCh38 chr11: 102,602,129-102,602,129 , GRCh37.p13 chr11: 102,472,860-102,472,860 MMP20
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5588927copy number variation1nstd207human GRCh38 chr11: 102,601,115-102,601,430 , GRCh37.p13 chr11: 102,471,846-102,472,161 MMP20
    nsv5511732copy number variation1nstd206human GRCh38 chr11: 102,601,127-102,601,431 , GRCh37.p13 chr11: 102,471,858-102,472,162 MMP20
    nsv5510107copy number variation1nstd206human GRCh38 chr11: 102,588,795-102,588,873 , GRCh37.p13 chr11: 102,459,526-102,459,604 MMP20
    nsv5499910copy number variation1nstd206human GRCh38 chr11: 102,578,287-102,579,425 , GRCh37.p13 chr11: 102,449,018-102,450,156 MMP20
    nsv5383321mobile element deletion2nstd186human GRCh37 chr11: 102,471,858-102,472,162 , GRCh38.p12 chr11: 102,601,127-102,601,431 MMP20
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5268896copy number variation1nstd204human GRCh38.p13 chr11: 102,601,101-102,601,400 , GRCh37.p13 chr11: 102,471,832-102,472,131 MMP20
    nsv5201047mobile element deletion1nstd204human GRCh38.p13 chr11: 102,601,127-102,601,431 , GRCh37.p13 chr11: 102,471,858-102,472,162 MMP20
    nsv5139280mobile element insertion1nstd203human GRCh38 chr11: 102,600,073-102,600,083 , GRCh37.p13 chr11: 102,470,804-102,470,814 MMP20
    nsv5137989mobile element insertion1nstd203human GRCh38 chr11: 102,602,129-102,602,129 , GRCh37.p13 chr11: 102,472,860-102,472,860 MMP20
    nsv5137444mobile element insertion1nstd203human GRCh38 chr11: 102,602,094-102,602,128 , GRCh37.p13 chr11: 102,472,825-102,472,859 MMP20
    nsv5137192mobile element insertion1nstd203human GRCh38 chr11: 102,601,125-102,601,150 , GRCh37.p13 chr11: 102,471,856-102,471,881 MMP20
    nsv5135094mobile element insertion1nstd203human GRCh38 chr11: 102,602,268-102,602,268 , GRCh37.p13 chr11: 102,472,999-102,472,999 MMP20
    nsv5133232mobile element insertion1nstd203human GRCh38 chr11: 102,602,130-102,602,130 , GRCh37.p13 chr11: 102,472,861-102,472,861 MMP20
    nsv5132512mobile element insertion1nstd203human GRCh38 chr11: 102,601,150-102,601,188 , GRCh37.p13 chr11: 102,471,881-102,471,919 MMP20
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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