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 546

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LOC105373207, LOC105373210, 113 more genes
    nsv5960684insertion1nstd209human GRCh38 chr1: 236,447,233-236,447,233 , GRCh37.p13 chr1: 236,610,533-236,610,533 EDARADD
    nsv5886772copy number variation1nstd209human GRCh38 chr1: 236,437,271-236,623,756 , GRCh37.p13 chr1: 236,600,571-236,787,056 , ENO1P1, 4 more genes
    nsv5886691copy number variation1nstd209human GRCh38 chr1: 236,428,628-236,428,704 , GRCh37.p13 chr1: 236,591,928-236,592,004 EDARADD
    nsv5881003copy number variation1nstd209human GRCh38 chr1: 236,473,274-236,473,335 , GRCh37.p13 chr1: 236,636,574-236,636,635 EDARADD
    nsv5877619copy number variation1nstd209human GRCh38 chr1: 236,431,625-236,431,949 , GRCh37.p13 chr1: 236,594,925-236,595,249 EDARADD
    nsv5870257copy number variation1nstd209human GRCh38 chr1: 236,420,806-236,421,561 , GRCh37.p13 chr1: 236,584,106-236,584,861 EDARADD
    nsv5829498copy number variation1nstd209human GRCh38 chr1: 236,450,851-236,453,150 , GRCh37.p13 chr1: 236,614,151-236,616,450 EDARADD
    nsv5829497copy number variation1nstd209human GRCh38 chr1: 236,438,379-236,452,675 , GRCh37.p13 chr1: 236,601,679-236,615,975 EDARADD
    nsv5720919mobile element insertion1nstd211human GRCh38 chr1: 236,399,020-236,399,020 , GRCh37.p13 chr1: 236,562,320-236,562,320 EDARADD
    nsv5607992insertion1nstd207human GRCh38 chr1: 236,447,242-236,447,242 , GRCh37.p13 chr1: 236,610,542-236,610,542 EDARADD
    nsv5576767copy number variation1nstd207human GRCh38 chr1: 236,478,259-236,478,363 , GRCh37.p13 chr1: 236,641,559-236,641,663 EDARADD
    nsv5573854copy number variation1nstd207human GRCh38 chr1: 236,431,625-236,431,949 , GRCh37.p13 chr1: 236,594,925-236,595,249 EDARADD
    nsv5566801copy number variation1nstd207human GRCh38 chr1: 236,420,806-236,421,561 , GRCh37.p13 chr1: 236,584,106-236,584,861 EDARADD
    nsv5554982mobile element insertion1nstd206human GRCh38 chr1: 236,399,020-236,399,071 , GRCh37.p13 chr1: 236,562,320-236,562,371 EDARADD
    nsv5538844insertion1nstd206human GRCh38 chr1: 236,432,244-236,432,266 , GRCh37.p13 chr1: 236,595,544-236,595,566 EDARADD
    nsv5452331copy number variation1nstd206human GRCh38 chr1: 236,422,065-236,422,122 , GRCh37.p13 chr1: 236,585,365-236,585,422 EDARADD
    nsv5448868copy number variation1nstd206human GRCh38 chr1: 236,478,259-236,478,364 , GRCh37.p13 chr1: 236,641,559-236,641,664 EDARADD
    nsv5448641copy number variation1nstd206human GRCh38 chr1: 236,427,575-236,428,338 , GRCh37.p13 chr1: 236,590,875-236,591,638 EDARADD
    nsv5441255copy number variation1nstd206human GRCh38 chr1: 236,473,276-236,473,336 , GRCh37.p13 chr1: 236,636,576-236,636,636 EDARADD
    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