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 74

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882822copy number variation1nstd102humanBenign GRCh37 chr3: 192,105,055-192,155,879 , GRCh38.p12 chr3: 192,387,266-192,438,090 FGF12
    nsv3886501copy number variation1nstd102humanBenign GRCh37 chr3: 192,302,970-192,312,755 , GRCh38.p12 chr3: 192,585,181-192,594,966 FGF12
    nsv3878712copy number variation1nstd102humanBenign GRCh37 chr3: 191,888,379-191,891,123 , GRCh38.p12 chr3: 192,170,590-192,173,334 FGF12
    nsv3876221copy number variation1nstd102humanBenign GRCh37 chr3: 192,389,300-192,392,000 , GRCh38.p12 chr3: 192,671,511-192,674,211 FGF12
    nsv3873532copy number variation1nstd102humanBenign GRCh37 chr3: 191,890,256-191,891,123 , GRCh38.p12 chr3: 192,172,467-192,173,334 FGF12
    nsv3874843copy number variation1nstd102humanBenign GRCh37 chr3: 192,122,744-192,123,264 , GRCh38.p12 chr3: 192,404,955-192,405,475 FGF12
    nsv6314731copy number variation2nstd102humanUncertain significance, Likely benign GRCh37 chr3: 192,053,130-192,126,012 , GRCh38.p12 chr3: 192,335,341-192,408,223 FGF12
    nsv6636441copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,101,116-192,156,513 , GRCh38.p12 chr3: 192,383,327-192,438,724 FGF12
    nsv4454857copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,100,736-192,155,879 , GRCh38.p12 chr3: 192,382,947-192,438,090 FGF12
    nsv3875867copy number variation1nstd102humannot provided GRCh38 chr3: 192,587,419-192,594,481 , GRCh37 chr3: 192,305,208-192,312,270 FGF12
    nsv6311867copy number variation2nstd102humanUncertain significance GRCh37 chr3: 192,125,794-192,126,012 , GRCh38.p12 chr3: 192,408,005-192,408,223 FGF12
    nsv7097187copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,861,798-191,888,465 , GRCh38.p12 chr3: 192,144,009-192,170,676 FGF12
    esv3648161copy number variation1estd216humannot provided GRCh37 chr3: 192,305,208-192,312,270 , GRCh38.p12 chr3: 192,587,419-192,594,481 FGF12
    nsv6311974copy number variation2nstd102humanUncertain significance, Likely pathogenic GRCh37 chr3: 191,888,227-192,126,012 , GRCh38.p12 chr3: 192,170,438-192,408,223 FGF12, FGF12-AS1
    nsv3875095copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,045,727-192,283,390 , GRCh38.p12 chr3: 192,327,938-192,565,601 FGF12, FGF12-AS2
    nsv3910808copy number variation1nstd102humanUncertain significance NCBI36 chr3: 193,542,372-193,749,243 , GRCh37 chr3: 192,059,678-192,266,549 , GRCh38 chr3: 192,341,889-192,548,760 FGF12, FGF12-AS2
    nsv3880966copy number variation1nstd102humanUncertain significance GRCh37 chr3: 191,916,059-192,044,332 , GRCh38.p12 chr3: 192,198,270-192,326,543 FGF12, FGF12-AS1
    nsv3871833copy number variation1nstd102humanBenign GRCh37 chr3: 191,866,779-192,456,208 , GRCh38.p12 chr3: 192,148,990-192,738,419 FGF12, FGF12-AS1, 3 more genes
    nsv3877092copy number variation1nstd102humanBenign GRCh37 chr3: 192,407,268-192,601,876 , GRCh38.p12 chr3: 192,689,479-192,884,087 FGF12, LOC107986056, 2 more genes
    nsv4455016copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,406,314-192,568,208 , GRCh38.p12 chr3: 192,688,525-192,850,419 FGF12, MB21D2, 2 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