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 859

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963932insertion1nstd209human GRCh38 chr7: 158,810,997-158,810,997 , GRCh37.p13 chr7: 158,603,688-158,603,688 ESYT2
    nsv5957406insertion1nstd209human GRCh38 chr7: 158,729,729-158,729,729 , GRCh37.p13 chr7: 158,522,420-158,522,420 ESYT2
    nsv5926947copy number variation1nstd209human GRCh38 chr7: 158,796,949-158,797,095 , GRCh37.p13 chr7: 158,589,640-158,589,786 ESYT2
    nsv5922049copy number variation1nstd209human GRCh38 chr7: 158,789,810-158,789,887 , GRCh37.p13 chr7: 158,582,501-158,582,578 ESYT2
    nsv5921133copy number variation1nstd209human GRCh38 chr7: 158,744,785-158,745,086 , GRCh37.p13 chr7: 158,537,476-158,537,777 ESYT2
    nsv5918874copy number variation1nstd209human GRCh38 chr7: 158,828,761-158,828,971 , GRCh37.p13 chr7: 158,621,452-158,621,662 ESYT2
    nsv5916271copy number variation1nstd209human GRCh38 chr7: 158,806,061-158,806,132 , GRCh37.p13 chr7: 158,598,752-158,598,823 ESYT2
    nsv5914335copy number variation1nstd209human GRCh38 chr7: 158,782,339-158,782,486 , GRCh37.p13 chr7: 158,575,030-158,575,177 , ESYT2
    nsv5911943copy number variation1nstd209human GRCh38 chr7: 158,763,969-158,764,035 , GRCh37.p13 chr7: 158,556,660-158,556,726 ESYT2
    nsv5911200copy number variation1nstd209human GRCh38 chr7: 158,782,401-158,782,452 , GRCh37.p13 chr7: 158,575,092-158,575,143 , ESYT2
    nsv5911075copy number variation1nstd209human GRCh38 chr7: 158,804,750-158,804,819 , GRCh37.p13 chr7: 158,597,441-158,597,510 ESYT2
    nsv5910568copy number variation1nstd209human GRCh38 chr7: 158,807,032-158,816,712 , GRCh37.p13 chr7: 158,599,723-158,609,403 ESYT2
    nsv5908547copy number variation1nstd209human GRCh38 chr7: 158,729,286-158,729,670 , GRCh37.p13 chr7: 158,521,977-158,522,361 ESYT2
    nsv5863515copy number variation1nstd209human GRCh38 chr7: 158,810,061-158,811,160 , GRCh37.p13 chr7: 158,602,752-158,603,851 ESYT2
    nsv5855106copy number variation1nstd209human GRCh38 chr7: 158,807,061-158,813,960 , GRCh37.p13 chr7: 158,599,752-158,606,651 ESYT2
    nsv5718985mobile element insertion1nstd211human GRCh38 chr7: 158,775,010-158,775,010 , GRCh37.p13 chr7: 158,567,701-158,567,701 ESYT2
    nsv5718439mobile element insertion1nstd211human GRCh38 chr7: 158,774,998-158,774,998 , GRCh37.p13 chr7: 158,567,689-158,567,689 ESYT2
    nsv5703777mobile element insertion2nstd211human GRCh38 chr7: 158,811,015-158,811,015 , GRCh37.p13 chr7: 158,603,706-158,603,706 ESYT2
    nsv5695606mobile element insertion2nstd211human GRCh38 chr7: 158,814,305-158,814,305 , GRCh37.p13 chr7: 158,606,996-158,606,996 ESYT2
    nsv5641410insertion1nstd207human GRCh38 chr7: 158,810,997-158,810,997 , GRCh37.p13 chr7: 158,603,688-158,603,688 ESYT2
    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