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 238

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073286inversion1nstd229human GRCh38 chr16: 84,799,664-85,287,657 , GRCh37.p13 chr16: 84,833,270-85,321,263 LOC123862, MIR12128, 13 more genes
    nsv7068302inversion1nstd229human GRCh38 chr16: 85,109,343-85,150,401 , GRCh37.p13 chr16: 85,142,949-85,184,007 LOC105371381, CIBAR2, 2 more genes
    nsv6993674copy number variation1nstd229human GRCh38 chr16: 85,149,101-85,291,800 , GRCh37.p13 chr16: 85,182,707-85,325,406 GSE1, LINC02139, 4 more genes
    nsv6990594copy number variation1nstd229human GRCh38 chr16: 85,123,538-85,138,388 , GRCh37.p13 chr16: 85,157,144-85,171,994 LOC105371381, LINC02139
    nsv6988186copy number variation1nstd229human GRCh38 chr16: 84,765,972-85,486,232 , GRCh37.p13 chr16: 84,799,578-85,519,838 KIAA0513, MIR5093, 17 more genes
    nsv6985778copy number variation1nstd229human GRCh38 chr16: 84,931,263-85,452,308 , GRCh37.p13 chr16: 84,964,869-85,485,914 KIAA0513, MIR12128, 12 more genes
    nsv6984541copy number variation1nstd229human GRCh38 chr16: 85,144,801-85,163,400 , GRCh37.p13 chr16: 85,178,407-85,197,006 LOC105371382, LINC02139
    nsv6984456copy number variation1nstd229human GRCh38 chr16: 85,067,868-85,267,059 , GRCh37.p13 chr16: 85,101,474-85,300,665 KIAA0513, MIR12128, 5 more genes
    nsv6984346copy number variation1nstd229human GRCh38 chr16: 84,940,101-85,330,600 , GRCh37.p13 chr16: 84,973,707-85,364,206 LOC101928502, LOC107984830, 12 more genes
    nsv6984163copy number variation1nstd229human GRCh38 chr16: 85,142,364-85,459,522 , GRCh37.p13 chr16: 85,175,970-85,493,128 GSE1, MIR5093, 7 more genes
    nsv6981941copy number variation1nstd229human GRCh38 chr16: 85,146,540-85,230,557 , GRCh37.p13 chr16: 85,180,146-85,264,163 LINC02139, LOC105371382, 2 more genes
    nsv6980319copy number variation1nstd229human GRCh38 chr16: 84,592,847-85,544,248 , GRCh37.p13 chr16: 84,626,453-85,577,854 COX6CP16, LINC02176, 20 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623995copy number variation1nstd224human GRCh37 chr16: 85,166,890-85,182,087 , GRCh38.p12 chr16: 85,133,284-85,148,481 LOC105371382, LINC02139
    nsv6590742inversion1nstd223human GRCh38 chr16: 83,952,013-85,834,110 , GRCh37.p13 chr16: 83,985,618-85,867,716 LOC101928502, LOC105371382, 47 more genes
    nsv6576050inversion1nstd223human GRCh38 chr16: 85,109,343-85,150,404 , GRCh37.p13 chr16: 85,142,949-85,184,010 CIBAR2, LINC02139, 2 more genes
    nsv6513750copy number variation1nstd223human GRCh38 chr16: 85,068,657-85,218,092 , GRCh37.p13 chr16: 85,102,263-85,251,698 GSE1, LINC02139, 5 more genes
    nsv6509790copy number variation1nstd223human GRCh38 chr16: 85,053,893-85,216,291 , GRCh37.p13 chr16: 85,087,499-85,249,897 KIAA0513, GSE1, 5 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6314016copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,134,463-85,705,611 , GRCh38.p12 chr16: 84,100,858-85,672,005 DNAAF1, COTL1, 34 more genes
    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