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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711476mobile element insertion2nstd211human GRCh38 chr11: 62,422,453-62,422,453 , GRCh37.p13 chr11: 62,189,925-62,189,925 LOC102723765, SCGB1A1
    nsv5653368insertion1nstd207human GRCh38 chr11: 62,422,438-62,422,438 , GRCh37.p13 chr11: 62,189,910-62,189,910 LOC102723765, SCGB1A1
    nsv5502835copy number variation1nstd206human GRCh38 chr11: 62,420,999-62,421,070 , GRCh37.p13 chr11: 62,188,471-62,188,542 LOC102723765, SCGB1A1
    nsv5412588mobile element insertion1nstd206human GRCh38 chr11: 62,422,453-62,422,504 , GRCh37.p13 chr11: 62,189,925-62,189,976 LOC102723765, SCGB1A1
    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
    nsv5138552mobile element insertion1nstd203human GRCh38 chr11: 62,422,443-62,422,453 , GRCh37.p13 chr11: 62,189,915-62,189,925 SCGB1A1, LOC102723765
    nsv5137288mobile element insertion1nstd203human GRCh38 chr11: 62,422,440-62,422,449 , GRCh37.p13 chr11: 62,189,912-62,189,921 SCGB1A1, LOC102723765
    nsv5135108mobile element insertion1nstd203human GRCh38 chr11: 62,422,442-62,422,453 , GRCh37.p13 chr11: 62,189,914-62,189,925 SCGB1A1, LOC102723765
    nsv5132379mobile element insertion1nstd203human GRCh38 chr11: 62,422,444-62,422,453 , GRCh37.p13 chr11: 62,189,916-62,189,925 SCGB1A1, LOC102723765
    nsv5131432mobile element insertion1nstd203human GRCh38 chr11: 62,422,445-62,422,453 , GRCh37.p13 chr11: 62,189,917-62,189,925 SCGB1A1, LOC102723765
    nsv5123300mobile element insertion1nstd203human GRCh38 chr11: 62,422,441-62,422,453 , GRCh37.p13 chr11: 62,189,913-62,189,925 LOC102723765, SCGB1A1
    nsv5120181mobile element insertion1nstd203human GRCh38 chr11: 62,422,438-62,422,453 , GRCh37.p13 chr11: 62,189,910-62,189,925 LOC102723765, SCGB1A1
    nsv4985014copy number variation1nstd200human GRCh38 chr11: 62,409,156-62,420,462 , GRCh37.p13 chr11: 62,176,628-62,187,934 SCGB1A1, LOC102723765
    nsv4979692copy number variation1nstd200human GRCh38 chr11: 62,422,822-62,425,865 , GRCh37.p13 chr11: 62,190,294-62,193,337 LOC102723765, SCGB1A1
    nsv4830383copy number variation1nstd200human GRCh37 chr11: 62,190,294-62,193,345 , GRCh38.p12 chr11: 62,422,822-62,425,873 LOC102723765, SCGB1A1
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4750858insertion1nstd199human GRCh37 chr11: 62,189,912-62,189,912 , GRCh38.p12 chr11: 62,422,440-62,422,440 SCGB1A1, LOC102723765
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729555copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,874,941-62,236,378 , GRCh38.p12 chr11: 62,107,469-62,468,906 INCENP, SCGB2A1, 11 more genes
    nsv4726303insertion1nstd186human GRCh37 chr11: 62,189,910-62,189,910 , GRCh38.p12 chr11: 62,422,438-62,422,438 SCGB1A1, LOC102723765
    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