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 209

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5967184insertion1nstd209human GRCh38 chr4: 18,192,723-18,192,723 , GRCh37.p13 chr4: 18,194,346-18,194,346 LOC107986262
    nsv5720545mobile element insertion2nstd211human GRCh38 chr4: 18,192,734-18,192,734 , GRCh37.p13 chr4: 18,194,357-18,194,357 LOC107986262
    nsv5684732mobile element insertion2nstd211human GRCh38 chr4: 18,167,894-18,167,894 , GRCh37.p13 chr4: 18,169,517-18,169,517 LOC107986262
    nsv5624307insertion1nstd207human GRCh38 chr4: 18,192,723-18,192,723 , GRCh37.p13 chr4: 18,194,346-18,194,346 LOC107986262
    nsv5555018mobile element insertion1nstd206human GRCh38 chr4: 18,192,734-18,192,785 , GRCh37.p13 chr4: 18,194,357-18,194,408 LOC107986262
    nsv5554140inversion1nstd206human GRCh38 chr4: 18,175,343-18,269,904 , GRCh37.p13 chr4: 18,176,966-18,271,527 LOC107986262
    nsv5407726mobile element insertion1nstd206human GRCh38 chr4: 18,167,894-18,167,945 , GRCh37.p13 chr4: 18,169,517-18,169,568 LOC107986262
    nsv5175401mobile element insertion1nstd203human GRCh38 chr4: 18,192,720-18,192,734 , GRCh37.p13 chr4: 18,194,343-18,194,357 LOC107986262
    nsv5175379mobile element insertion1nstd203human GRCh38 chr4: 18,192,723-18,192,734 , GRCh37.p13 chr4: 18,194,346-18,194,357 LOC107986262
    nsv5166959mobile element insertion1nstd203human GRCh38 chr4: 18,192,730-18,192,730 , GRCh37.p13 chr4: 18,194,353-18,194,353 LOC107986262
    nsv5166054mobile element insertion1nstd203human GRCh38 chr4: 18,192,721-18,192,736 , GRCh37.p13 chr4: 18,194,344-18,194,359 LOC107986262
    nsv5161256mobile element insertion1nstd203human GRCh38 chr4: 18,192,728-18,192,730 , GRCh37.p13 chr4: 18,194,351-18,194,353 LOC107986262
    nsv5160092mobile element insertion1nstd203human GRCh38 chr4: 18,192,729-18,192,734 , GRCh37.p13 chr4: 18,194,352-18,194,357 LOC107986262
    nsv5098316mobile element insertion1nstd203human GRCh38 chr4: 18,167,879-18,167,894 , GRCh37.p13 chr4: 18,169,502-18,169,517 LOC107986262
    nsv5087240mobile element insertion1nstd203human GRCh38 chr4: 18,167,884-18,167,894 , GRCh37.p13 chr4: 18,169,507-18,169,517 LOC107986262
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4921754copy number variation1nstd200human GRCh38 chr4: 18,212,254-18,216,170 , GRCh37.p13 chr4: 18,213,877-18,217,793 LOC107986262
    nsv4921753copy number variation1nstd200human GRCh38 chr4: 18,191,622-18,192,498 , GRCh37.p13 chr4: 18,193,245-18,194,121 LOC107986262
    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