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 2226

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137160copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 41,241,162-41,274,831 , GRCh38.p12 chr3: 41,199,671-41,233,340 CTNNB1
    nsv3893624copy number variation1nstd102humanBenign GRCh37 chr9: 112,823,818-112,830,706 , GRCh38.p12 chr9: 110,061,538-110,068,426 PALM2AKAP2
    nsv3895683copy number variation1nstd102humanBenign GRCh37 chr9: 112,826,429-112,830,706 , GRCh38.p12 chr9: 110,064,149-110,068,426 PALM2AKAP2
    nsv7093066copy number variation1nstd102humanUncertain significance GRCh37 chr13: 33,590,495-33,590,602 , GRCh38 chr13: 33,016,357-33,016,464 KL
    nsv7093180copy number variation1nstd102humanUncertain significance GRCh37 chr13: 33,590,493-33,590,597 , GRCh38 chr13: 33,016,355-33,016,459 KL
    esv4004549copy number variation1estd231human GRCh37 chr9: 112,430,200-112,430,515 , GRCh38.p12 chr9: 109,667,920-109,668,235 PALM2AKAP2
    esv4008167copy number variation1estd231human GRCh37 chr9: 112,716,114-112,716,941 , GRCh38.p12 chr9: 109,953,834-109,954,661 PALM2AKAP2
    nsv6921639copy number variation1nstd229human GRCh38 chr12: 88,473,773-88,518,443 , GRCh37.p13 chr12: 88,867,550-88,912,220 KITLG
    nsv6859729copy number variation1nstd229human GRCh38 chr9: 110,072,237-110,110,352 , GRCh37.p13 chr9: 112,834,517-112,872,632 PALM2AKAP2
    nsv6870518copy number variation1nstd229human GRCh38 chr9: 109,984,255-110,014,929 , GRCh37.p13 chr9: 112,746,535-112,777,209 PALM2AKAP2
    nsv6862360copy number variation1nstd229human GRCh38 chr9: 109,649,087-109,679,341 , GRCh37.p13 chr9: 112,411,367-112,441,621 PALM2AKAP2
    nsv6874953copy number variation1nstd229human GRCh38 chr9: 109,682,026-109,696,142 , GRCh37.p13 chr9: 112,444,306-112,458,422 PALM2AKAP2
    nsv6862642copy number variation1nstd229human GRCh38 chr9: 109,829,582-109,842,592 , GRCh37.p13 chr9: 112,591,862-112,604,872 PALM2AKAP2
    nsv6871237copy number variation1nstd229human GRCh38 chr9: 109,676,041-109,686,267 , GRCh37.p13 chr9: 112,438,321-112,448,547 PALM2AKAP2
    nsv6864070copy number variation1nstd229human GRCh38 chr9: 110,109,286-110,119,151 , GRCh37.p13 chr9: 112,871,566-112,881,431 PALM2AKAP2
    nsv6869953copy number variation1nstd229human GRCh38 chr9: 109,928,831-109,937,842 , GRCh37.p13 chr9: 112,691,111-112,700,122 PALM2AKAP2
    nsv6921895copy number variation1nstd229human GRCh38 chr12: 88,562,901-88,570,600 , GRCh37.p13 chr12: 88,956,678-88,964,377 KITLG
    nsv6950623copy number variation1nstd229human GRCh38 chr13: 33,028,401-33,035,800 , GRCh37.p13 chr13: 33,602,539-33,609,937 KL
    nsv6869802copy number variation1nstd229human GRCh38 chr9: 109,660,840-109,667,246 , GRCh37.p13 chr9: 112,423,120-112,429,526 PALM2AKAP2
    nsv6924186copy number variation1nstd229human GRCh38 chr12: 88,559,877-88,566,225 , GRCh37.p13 chr12: 88,953,654-88,960,002 KITLG
    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