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 238

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895123copy number variation1nstd102humanBenign GRCh37 chr7: 158,880,597-158,883,667 , GRCh38.p12 chr7: 159,087,906-159,090,976 VIPR2
    nsv3905519copy number variation1nstd102humanBenign GRCh37 chr19: 17,007,351-17,007,551 , GRCh38.p12 chr19: 16,896,540-16,896,740 CPAMD8
    nsv3908334copy number variation1nstd102humanBenign GRCh37 chr7: 158,850,355-158,935,236 , GRCh38.p12 chr7: 159,057,664-159,142,544 VIPR2
    nsv3914506copy number variation1nstd102humanLikely benign NCBI36 chr7: 158,534,591-158,612,949 , GRCh38 chr7: 159,049,139-159,127,497 , GRCh37 chr7: 158,841,830-158,920,188 VIPR2
    nsv4456758copy number variation1nstd102humanUncertain significance GRCh37 chr7: 158,901,052-159,019,897 , GRCh38.p12 chr7: 159,108,361-159,227,207 VIPR2
    nsv7098992copy number variation1nstd102humanPathogenic GRCh37 chr3: 8,775,485-8,788,452 , GRCh38.p12 chr3: 8,733,799-8,746,766 CAV3, SSUH2
    nsv4451192copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr3: 8,775,553-8,787,563 , GRCh38 chr3: 8,733,867-8,745,877 CAV3, SSUH2
    nsv3877830copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 159,061,689-159,335,973 , GRCh37.p13 chr7: 158,854,380-159,128,663 VIPR2, PIP5K1P2
    nsv3916190copy number variation1nstd102humanLikely benign NCBI36 chr7: 158,534,664-158,821,317 , GRCh38 chr7: 159,049,212-159,335,866 , GRCh37 chr7: 158,841,903-159,128,556 VIPR2, PIP5K1P2
    nsv3901289copy number variation1nstd102humanBenign GRCh37 chr7: 158,883,123-159,122,532 , GRCh38.p12 chr7: 159,090,432-159,329,842 VIPR2, PIP5K1P2
    nsv3909981copy number variation1nstd102humanLikely benign NCBI36 chr7: 158,534,591-158,750,796 , GRCh37 chr7: 158,841,830-159,058,035 , GRCh38 chr7: 159,049,139-159,265,346 VIPR2, PIP5K1P2
    nsv3924092copy number variation1nstd102humanLikely benign NCBI36 chr7: 158,620,930-158,719,401 , GRCh37 chr7: 158,928,169-159,026,640 , GRCh38 chr7: 159,135,478-159,233,950 PIP5K1P2, VIPR2
    nsv3878851copy number variation1nstd102humannot provided GRCh37 chr3: 8,775,496-8,788,451 , GRCh38 chr3: 8,733,810-8,746,765 SSUH2, CAV3
    nsv6635973copy number variation1nstd102humannot provided GRCh37 chr3: 8,775,677-8,810,000 , GRCh38 chr3: 8,733,991-8,745,868 SSUH2, CAV3
    nsv3878570copy number variation1nstd102humannot provided GRCh37 chr7: 158,845,384-159,119,486 , GRCh38.p12 chr7: 159,052,693-159,326,796 PIP5K1P2, VIPR2
    nsv4456983copy number variation1nstd102humanUncertain significance GRCh37 chr7: 158,920,184-159,038,489 , GRCh38.p12 chr7: 159,127,493-159,245,799 PIP5K1P2, VIPR2
    esv3648399copy number variation1estd216humannot provided GRCh37 chr7: 158,845,384-159,119,486 , GRCh38.p12 chr7: 159,052,693-159,326,796 VIPR2, PIP5K1P2
    nsv3898379copy number variation1nstd102humanPathogenic GRCh37 chr7: 158,649,005-159,126,310 , GRCh38.p12 chr7: 158,856,314-159,333,620 VIPR2, DYNC2I1, 2 more genes
    nsv3883570copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr7: 158,519,118-158,986,159 , GRCh38 chr7: 158,726,427-159,193,469 VIPR2, DYNC2I1, 2 more genes
    nsv3911106copy number variation1nstd102humanLikely benign NCBI36 chr7: 158,347,062-158,812,468 , GRCh37 chr7: 158,654,301-159,119,707 , GRCh38 chr7: 158,861,610-159,327,017 LINC00689, VIPR2, 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