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 186

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117777copy number variation1nstd186human GRCh37 chr3: 194,068,576-194,068,859 , GRCh38.p12 chr3: 194,347,847-194,348,130 CPN2
    nsv5893542copy number variation1nstd209human GRCh38 chr3: 194,347,638-194,347,689 , GRCh37.p13 chr3: 194,068,367-194,068,418 CPN2
    nsv5572292copy number variation1nstd207human GRCh38 chr3: 194,347,785-194,347,862 , GRCh37.p13 chr3: 194,068,514-194,068,591 CPN2
    nsv5571385copy number variation1nstd207human GRCh38 chr3: 194,347,853-194,348,210 , GRCh37.p13 chr3: 194,068,582-194,068,939 CPN2
    nsv5552511insertion1nstd206human GRCh38 chr3: 194,344,089-194,344,140 , GRCh37.p13 chr3: 194,064,818-194,064,869 CPN2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5453332copy number variation1nstd206human GRCh38 chr3: 194,338,805-194,339,175 , GRCh37.p13 chr3: 194,059,534-194,059,904 CPN2
    nsv5450820copy number variation1nstd206human GRCh38 chr3: 194,347,827-194,348,150 , GRCh37.p13 chr3: 194,068,556-194,068,879 CPN2
    nsv5450578copy number variation1nstd206human GRCh38 chr3: 194,350,415-194,350,862 , GRCh37.p13 chr3: 194,071,144-194,071,591 CPN2
    nsv5387866copy number variation1nstd186human GRCh37 chr3: 194,068,534-194,068,945 , GRCh38.p12 chr3: 194,347,805-194,348,216 CPN2
    nsv5386826copy number variation1nstd186human GRCh37 chr3: 194,068,419-194,068,940 , GRCh38.p12 chr3: 194,347,690-194,348,211 CPN2
    nsv5311250copy number variation1nstd204human GRCh38.p13 chr3: 194,347,596-194,348,381 , GRCh37.p13 chr3: 194,068,325-194,069,110 CPN2
    nsv5234391copy number variation1nstd204human GRCh38.p13 chr3: 194,347,801-194,348,300 , GRCh37.p13 chr3: 194,068,530-194,069,029 CPN2
    nsv5214643mobile element deletion1nstd204human GRCh38.p13 chr3: 194,338,828-194,339,161 , GRCh37.p13 chr3: 194,059,557-194,059,890 CPN2
    nsv5084625mobile element insertion1nstd203human GRCh38 chr3: 194,345,327-194,345,344 , GRCh37.p13 chr3: 194,066,056-194,066,073 CPN2
    nsv4928323copy number variation1nstd200human GRCh38 chr3: 194,347,687-194,348,212 , GRCh37.p13 chr3: 194,068,416-194,068,941 CPN2
    nsv4928322copy number variation1nstd200human GRCh38 chr3: 194,347,663-194,348,002 , GRCh37.p13 chr3: 194,068,392-194,068,731 CPN2
    nsv4925015copy number variation1nstd200human GRCh38 chr3: 194,179,860-194,436,927 , GRCh37.p13 chr3: 193,897,649-194,157,656 CPN2, LINC00887, 6 more genes
    nsv4872251mobile element deletion1nstd200human GRCh38 chr3: 194,338,835-194,339,155 , GRCh37.p13 chr3: 194,059,564-194,059,884 CPN2
    nsv4807222copy number variation1nstd200human GRCh37 chr3: 194,068,525-194,068,951 , GRCh38.p12 chr3: 194,347,796-194,348,222 CPN2
    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