U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 41

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880042copy number variation1nstd102humanBenign GRCh37 chr6: 116,438,960-116,448,350 , GRCh38.p12 chr6: 116,117,797-116,127,187 COL10A1, NT5DC1
    nsv3889206copy number variation1nstd102humanBenign GRCh37 chr6: 116,442,327-116,448,350 , GRCh38.p12 chr6: 116,121,164-116,127,187 COL10A1, NT5DC1
    nsv3872201copy number variation1nstd102humanBenign GRCh37 chr6: 116,443,322-116,448,350 , GRCh38.p12 chr6: 116,122,159-116,127,187 COL10A1, NT5DC1
    nsv3875555copy number variation1nstd102humanBenign GRCh37 chr6: 116,443,447-116,448,350 , GRCh38.p12 chr6: 116,122,284-116,127,187 COL10A1, NT5DC1
    nsv3884969copy number variation1nstd102humanBenign GRCh37 chr6: 116,443,338-116,446,926 , GRCh38.p12 chr6: 116,122,175-116,125,763 COL10A1, NT5DC1
    nsv3875756copy number variation1nstd102humanBenign GRCh37 chr6: 116,445,914-116,448,350 , GRCh38.p12 chr6: 116,124,751-116,127,187 COL10A1, NT5DC1
    nsv3875524copy number variation1nstd102humanBenign GRCh37 chr6: 116,446,695-116,448,350 , GRCh38.p12 chr6: 116,125,532-116,127,187 COL10A1, NT5DC1
    nsv6312018copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,441,795-116,442,866 , GRCh38.p12 chr6: 116,120,632-116,121,703 COL10A1, NT5DC1
    nsv7093142copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,441,969-116,442,112 , GRCh38 chr6: 116,120,806-116,120,949 COL10A1, NT5DC1
    nsv6291305copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,480,702-116,577,174 , GRCh38.p12 chr6: 116,159,539-116,256,011 COL10A1, TSPYL4, 2 more genes
    nsv3884833copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,409,181-116,488,289 , GRCh38.p12 chr6: 116,088,018-116,167,126 COL10A1, NT5DC1, 2 more genes
    nsv4455195copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,371,057-116,515,290 , GRCh38.p12 chr6: 116,049,894-116,194,127 COL10A1, NT5DC1, 2 more genes
    nsv3880626copy number variation1nstd102humanPathogenic GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541 COL10A1, LOC107986534, 426 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 COL10A1, RN7SL509P, 311 more genes
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 COL10A1, TUBE1, 318 more genes
    nsv3920683copy number variation1nstd102humanPathogenic NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720 COL10A1, SSXP10, 298 more genes
    nsv3876958copy number variation1nstd102humanPathogenic GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766 COL10A1, LIN28B-AS1, 258 more genes
    nsv3910417copy number variation1nstd102humanPathogenic GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300 COL10A1, LINC02518, 266 more genes
    nsv3924741copy number variation1nstd102humanPathogenic GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058 COL10A1, LOC105377979, 266 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 COL10A1, SLC18B1, 223 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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