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 188

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7043607inversion1nstd229human GRCh38 chr6: 110,211,435-110,252,889 , GRCh37.p13 chr6: 110,532,638-110,574,092 CDC40, METTL24, 1 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6808917copy number variation1nstd229human GRCh38 chr6: 110,060,590-110,297,700 , GRCh37.p13 chr6: 110,381,793-110,618,903 LOC105377937, WASF1, 2 more genes
    nsv6805968copy number variation1nstd229human GRCh38 chr6: 110,201,183-110,206,307 , GRCh37.p13 chr6: 110,522,386-110,527,510 CDC40
    nsv6801754copy number variation1nstd229human GRCh38 chr6: 110,211,401-110,246,000 , GRCh37.p13 chr6: 110,532,604-110,567,203 LOC105377937, CDC40, 1 more genes
    nsv6801259copy number variation1nstd229human GRCh38 chr6: 110,203,301-110,209,800 , GRCh37.p13 chr6: 110,524,504-110,531,003 CDC40
    nsv6636674copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,504,179-110,635,478 , GRCh38.p12 chr6: 110,182,976-110,314,275 CDC40, METTL24, 1 more genes
    nsv6618246copy number variation1nstd223human GRCh38 chr6: 110,220,692-110,235,380 , GRCh37.p13 chr6: 110,541,895-110,556,583 CDC40
    nsv6602771copy number variation1nstd223human GRCh38 chr6: 110,201,242-110,201,794 , GRCh37.p13 chr6: 110,522,445-110,522,997 CDC40
    nsv6567864inversion1nstd223human GRCh38 chr6: 109,778,846-111,235,585 , GRCh37.p13 chr6: 110,100,049-111,556,788 RNU6-1115P, GSTM2P1, 33 more genes
    nsv6561962inversion1nstd223human GRCh38 chr6: 110,198,288-110,199,331 , GRCh37.p13 chr6: 110,519,491-110,520,534 CDC40
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
    nsv6303187copy number variation1nstd186human GRCh37 chr6: 110,541,821-110,556,513 , GRCh38.p12 chr6: 110,220,618-110,235,310 CDC40
    nsv6135706copy number variation1nstd213human GRCh37 chr6: 109,920,000-110,550,001 , GRCh38.p12 chr6: 109,598,797-110,228,798 GPR6, WASF1, 4 more genes
    nsv5691191mobile element insertion1nstd211human GRCh38 chr6: 110,217,165-110,217,165 , GRCh37.p13 chr6: 110,538,368-110,538,368 CDC40
    nsv5643474insertion1nstd207human GRCh38 chr6: 110,185,397-110,185,397 , GRCh37.p13 chr6: 110,506,600-110,506,600 CDC40
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5470633copy number variation1nstd206human GRCh38 chr6: 110,181,184-110,181,260 , GRCh37.p13 chr6: 110,502,387-110,502,463 CDC40
    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