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 550

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6638031copy number variation1nstd102humanUncertain significance GRCh37 chr12: 76,812,664-76,891,516 , GRCh38.p12 chr12: 76,418,884-76,497,736 OSBPL8
    nsv1398602copy number variation1nstd102humanUncertain significance GRCh37 chr12: 76,763,038-76,780,400 , GRCh38.p12 chr12: 76,369,258-76,386,620 OSBPL8
    nsv6922021copy number variation1nstd229human GRCh38 chr12: 76,460,818-76,480,798 , GRCh37.p13 chr12: 76,854,598-76,874,578 OSBPL8
    nsv6918484copy number variation1nstd229human GRCh38 chr12: 76,413,807-76,427,503 , GRCh37.p13 chr12: 76,807,587-76,821,283 OSBPL8
    nsv6928024copy number variation1nstd229human GRCh38 chr12: 76,511,801-76,521,800 , GRCh37.p13 chr12: 76,905,581-76,915,580 OSBPL8
    nsv6918626copy number variation1nstd229human GRCh38 chr12: 76,458,679-76,468,243 , GRCh37.p13 chr12: 76,852,459-76,862,023 OSBPL8
    nsv6935558copy number variation1nstd229human GRCh38 chr12: 76,430,490-76,438,807 , GRCh37.p13 chr12: 76,824,270-76,832,587 OSBPL8
    nsv6935502copy number variation1nstd229human GRCh38 chr12: 76,539,144-76,545,339 , GRCh37.p13 chr12: 76,932,924-76,939,119 OSBPL8
    nsv6937582copy number variation1nstd229human GRCh38 chr12: 76,491,809-76,497,970 , GRCh37.p13 chr12: 76,885,589-76,891,750 OSBPL8
    nsv6930967copy number variation1nstd229human GRCh38 chr12: 76,477,500-76,481,795 , GRCh37.p13 chr12: 76,871,280-76,875,575 OSBPL8
    nsv6933311copy number variation1nstd229human GRCh38 chr12: 76,379,363-76,383,326 , GRCh37.p13 chr12: 76,773,143-76,777,106 OSBPL8
    nsv6930551copy number variation1nstd229human GRCh38 chr12: 76,537,891-76,541,839 , GRCh37.p13 chr12: 76,931,671-76,935,619 OSBPL8
    nsv6934754copy number variation1nstd229human GRCh38 chr12: 76,359,065-76,362,565 , GRCh37.p13 chr12: 76,752,845-76,756,345 OSBPL8
    nsv6936052copy number variation1nstd229human GRCh38 chr12: 76,464,179-76,466,841 , GRCh37.p13 chr12: 76,857,959-76,860,621 OSBPL8
    nsv6919141copy number variation1nstd229human GRCh38 chr12: 76,403,825-76,406,448 , GRCh37.p13 chr12: 76,797,605-76,800,228 OSBPL8
    nsv6934740copy number variation1nstd229human GRCh38 chr12: 76,461,511-76,464,055 , GRCh37.p13 chr12: 76,855,291-76,857,835 OSBPL8
    nsv6933599copy number variation1nstd229human GRCh38 chr12: 76,510,564-76,512,962 , GRCh37.p13 chr12: 76,904,344-76,906,742 OSBPL8
    nsv6934845copy number variation1nstd229human GRCh38 chr12: 76,506,922-76,508,034 , GRCh37.p13 chr12: 76,900,702-76,901,814 OSBPL8
    nsv6924249copy number variation1nstd229human GRCh38 chr12: 76,507,516-76,508,023 , GRCh37.p13 chr12: 76,901,296-76,901,803 OSBPL8
    nsv6472746copy number variation1nstd223human GRCh38 chr12: 76,430,501-76,438,800 , GRCh37.p13 chr12: 76,824,281-76,832,580 OSBPL8
    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