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 754

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122947copy number variation1nstd186human GRCh37 chr9: 87,503,903-87,504,205 , GRCh38.p12 chr9: 84,888,988-84,889,290 NTRK2
    nsv5956859insertion1nstd209human GRCh38 chr9: 84,891,299-84,891,299 , GRCh37.p13 chr9: 87,506,214-87,506,214 NTRK2
    nsv5954718insertion1nstd209human GRCh38 chr9: 85,004,039-85,004,039 , GRCh37.p13 chr9: 87,618,954-87,618,954 NTRK2
    nsv5951763insertion1nstd209human GRCh38 chr9: 84,888,979-84,888,979 , GRCh37.p13 chr9: 87,503,894-87,503,894 NTRK2
    nsv5948084insertion1nstd209human GRCh38 chr9: 84,730,760-84,730,760 , GRCh37.p13 chr9: 87,345,675-87,345,675 NTRK2
    nsv5923083copy number variation1nstd209human GRCh38 chr9: 84,730,441-84,730,755 , GRCh37.p13 chr9: 87,345,356-87,345,670 NTRK2
    nsv5919808copy number variation1nstd209human GRCh38 chr9: 84,779,206-84,779,689 , GRCh37.p13 chr9: 87,394,121-87,394,604 NTRK2
    nsv5918506copy number variation1nstd209human GRCh38 chr9: 84,737,692-84,738,405 , GRCh37.p13 chr9: 87,352,607-87,353,320 NTRK2
    nsv5725786mobile element insertion1nstd211human GRCh38 chr9: 84,786,893-84,786,893 , GRCh37.p13 chr9: 87,401,808-87,401,808 NTRK2
    nsv5716085mobile element insertion1nstd211human GRCh38 chr9: 84,895,170-84,895,170 , GRCh37.p13 chr9: 87,510,085-87,510,085 NTRK2
    nsv5713149mobile element insertion2nstd211human GRCh38 chr9: 84,783,067-84,783,067 , GRCh37.p13 chr9: 87,397,982-87,397,982 NTRK2
    nsv5708399mobile element insertion1nstd211human GRCh38 chr9: 84,931,739-84,931,739 , GRCh37.p13 chr9: 87,546,654-87,546,654 NTRK2
    nsv5707314mobile element insertion1nstd211human GRCh38 chr9: 85,006,093-85,006,093 , GRCh37.p13 chr9: 87,621,008-87,621,008 NTRK2
    nsv5706387mobile element insertion2nstd211human GRCh38 chr9: 84,687,840-84,687,840 , GRCh37.p13 chr9: 87,302,755-87,302,755 NTRK2
    nsv5695634mobile element insertion2nstd211human GRCh38 chr9: 84,891,313-84,891,313 , GRCh37.p13 chr9: 87,506,228-87,506,228 NTRK2
    nsv5639198insertion1nstd207human GRCh38 chr9: 84,870,179-84,870,179 , GRCh37.p13 chr9: 87,485,094-87,485,094 NTRK2
    nsv5634290insertion1nstd207human GRCh38 chr9: 84,891,299-84,891,299 , GRCh37.p13 chr9: 87,506,214-87,506,214 NTRK2
    nsv5631994insertion1nstd207human GRCh38 chr9: 85,004,039-85,004,039 , GRCh37.p13 chr9: 87,618,954-87,618,954 NTRK2
    nsv5631088insertion1nstd207human GRCh38 chr9: 84,797,660-84,797,660 , GRCh37.p13 chr9: 87,412,575-87,412,575 NTRK2
    nsv5598776copy number variation1nstd207human GRCh38 chr9: 84,730,441-84,730,755 , GRCh37.p13 chr9: 87,345,356-87,345,670 NTRK2
    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