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 357

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7066250inversion1nstd229human GRCh38 chr18: 54,862,924-58,506,448 , GRCh37.p13 chr18: 52,530,155-56,173,680 NARS1, FECH, 48 more genes
    nsv7064485inversion1nstd229human GRCh38 chr18: 54,939,082-54,942,469 , GRCh37.p13 chr18: 52,606,313-52,609,700 CCDC68
    nsv7059189inversion1nstd229human GRCh38 chr18: 54,910,515-54,910,563 , GRCh37.p13 chr18: 52,577,746-52,577,794 CCDC68
    nsv7016052copy number variation1nstd229human GRCh38 chr18: 54,956,303-54,960,114 , GRCh37.p13 chr18: 52,623,534-52,627,345 CCDC68
    nsv7012428copy number variation1nstd229human GRCh38 chr18: 54,910,405-54,915,077 , GRCh37.p13 chr18: 52,577,636-52,582,308 CCDC68
    nsv7005316copy number variation1nstd229human GRCh38 chr18: 54,938,985-54,981,655 , GRCh37.p13 chr18: 52,606,216-52,648,886 CCDC68, MAP1LC3P
    nsv7001062copy number variation1nstd229human GRCh38 chr18: 54,917,047-54,920,795 , GRCh37.p13 chr18: 52,584,278-52,588,026 CCDC68
    nsv6998199copy number variation1nstd229human GRCh38 chr18: 54,927,483-54,929,908 , GRCh37.p13 chr18: 52,594,714-52,597,139 CCDC68
    nsv6637851copy number variation1nstd102humanUncertain significance GRCh37 chr18: 51,223,984-53,001,044 , GRCh38.p12 chr18: 53,697,614-55,333,813 MBD2, LINC03035, 15 more genes
    nsv6637722copy number variation1nstd102humanPathogenic GRCh37 chr18: 52,023,322-53,332,606 , GRCh38.p12 chr18: 54,496,952-55,665,375 LINC03035, DYNAP, 13 more genes
    nsv6529527copy number variation1nstd223human GRCh38 chr18: 54,943,001-54,943,600 , GRCh37.p13 chr18: 52,610,232-52,610,831 CCDC68
    nsv6529203copy number variation1nstd223human GRCh38 chr18: 54,950,889-54,951,207 , GRCh37.p13 chr18: 52,618,120-52,618,438 CCDC68
    nsv6527537copy number variation1nstd223human GRCh38 chr18: 54,899,245-54,899,596 , GRCh37.p13 chr18: 52,566,476-52,566,827 CCDC68
    nsv6515785copy number variation1nstd223human GRCh38 chr18: 54,959,201-54,959,800 , GRCh37.p13 chr18: 52,626,432-52,627,031 CCDC68
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314029copy number variation1nstd102humanPathogenic GRCh37 chr18: 50,707,829-54,924,248 , GRCh38.p12 chr18: 53,181,459-57,257,017 RNA5SP459, POLI, 42 more genes
    nsv6242476mobile element insertion1nstd215human GRCh38 chr18: 54,908,055-54,908,055 , GRCh37.p13 chr18: 52,575,286-52,575,286 CCDC68
    nsv6144954copy number variation1nstd206human GRCh38 chr18: 54,950,878-54,951,227 , GRCh37.p13 chr18: 52,618,109-52,618,458 CCDC68
    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