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 303

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094125copy number variation1nstd102humanUncertain significance GRCh37 chr12: 112,884,060-112,884,222 , GRCh38.p12 chr12: 112,446,256-112,446,418 PTPN11
    nsv7094028copy number variation1nstd102humanUncertain significance GRCh37 chr12: 112,910,728-113,008,334 , GRCh38.p12 chr12: 112,472,924-112,570,530 PTPN11
    nsv7094027copy number variation1nstd102humanPathogenic GRCh37 chr12: 112,909,300-112,915,437 , GRCh38.p12 chr12: 112,471,496-112,477,633 PTPN11
    nsv7093957copy number variation1nstd102humanUncertain significance GRCh37 chr12: 112,919,858-112,920,029 , GRCh38.p12 chr12: 112,482,054-112,482,225 PTPN11
    nsv7070180inversion1nstd229human GRCh38 chr12: 111,927,437-115,941,441 , GRCh37.p13 chr12: 112,365,241-116,379,246 OAS1, LHX5, 62 more genes
    nsv6937507copy number variation1nstd229human GRCh38 chr12: 112,028,701-112,494,400 , GRCh37.p13 chr12: 112,466,505-112,932,204 RN7SKP71, TRAFD1, 8 more genes
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6928599copy number variation1nstd229human GRCh38 chr12: 112,437,269-112,444,603 , GRCh37.p13 chr12: 112,875,073-112,882,407 PTPN11
    nsv6925783copy number variation1nstd229human GRCh38 chr12: 112,457,853-112,462,958 , GRCh37.p13 chr12: 112,895,657-112,900,762 PTPN11
    nsv6621499copy number variation1nstd224human GRCh37 chr12: 112,926,872-112,940,030 , GRCh38.p12 chr12: 112,489,068-112,502,226 PTPN11
    nsv6621406copy number variation1nstd224human GRCh37 chr12: 112,869,780-112,892,440 , GRCh38.p12 chr12: 112,431,976-112,454,636 PTPN11
    nsv6621405copy number variation1nstd224human GRCh37 chr12: 112,869,780-112,888,313 , GRCh38.p12 chr12: 112,431,976-112,450,509 PTPN11
    nsv6595014inversion1nstd223human GRCh38 chr12: 112,494,875-112,495,630 , GRCh37.p13 chr12: 112,932,679-112,933,434 PTPN11
    nsv6592481inversion1nstd223human GRCh38 chr12: 112,486,003-112,487,318 , GRCh37.p13 chr12: 112,923,807-112,925,122 PTPN11
    nsv6586863inversion1nstd223human GRCh38 chr12: 112,429,812-112,430,085 , GRCh37.p13 chr12: 112,867,616-112,867,889 PTPN11
    nsv6586389inversion1nstd223human GRCh38 chr12: 112,500,165-112,500,702 , GRCh37.p13 chr12: 112,937,969-112,938,506 PTPN11
    nsv6582461inversion1nstd223human GRCh38 chr12: 112,485,767-112,487,179 , GRCh37.p13 chr12: 112,923,571-112,924,983 PTPN11
    nsv6582122inversion1nstd223human GRCh38 chr12: 112,499,770-112,500,816 , GRCh37.p13 chr12: 112,937,574-112,938,620 PTPN11
    nsv6579897inversion1nstd223human GRCh38 chr12: 112,493,263-112,494,080 , GRCh37.p13 chr12: 112,931,067-112,931,884 PTPN11
    nsv6579795inversion1nstd223human GRCh38 chr12: 112,426,532-112,426,961 , GRCh37.p13 chr12: 112,864,336-112,864,765 PTPN11
    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