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 165

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115560mobile element insertion1nstd186human GRCh37 chr9: 116,095,573-116,095,624 , GRCh38.p12 chr9: 113,333,293-113,333,344 WDR31
    nsv5966976insertion1nstd209human GRCh38 chr9: 113,333,278-113,333,278 , GRCh37.p13 chr9: 116,095,558-116,095,558 WDR31
    nsv5860891copy number variation1nstd209human GRCh38 chr9: 113,322,176-113,324,920 , GRCh37.p13 chr9: 116,084,456-116,087,200 WDR31
    nsv5705455mobile element insertion2nstd211human GRCh38 chr9: 113,333,293-113,333,293 , GRCh37.p13 chr9: 116,095,573-116,095,573 WDR31
    nsv5643381insertion1nstd207human GRCh38 chr9: 113,333,278-113,333,278 , GRCh37.p13 chr9: 116,095,558-116,095,558 WDR31
    nsv5399401mobile element insertion1nstd206human GRCh38 chr9: 113,333,293-113,333,344 , GRCh37.p13 chr9: 116,095,573-116,095,624 WDR31
    nsv5319083copy number variation1nstd204human GRCh37.p13 chr9: 116,077,135-116,147,801 , GRCh38.p13 chr9: 113,314,855-113,385,521 ALAD, BSPRY, 2 more genes
    nsv5249891copy number variation1nstd204human GRCh38.p13 chr9: 113,314,876-113,344,891 , GRCh37.p13 chr9: 116,077,156-116,107,171 WDR31
    nsv5249518copy number variation1nstd204human GRCh38.p13 chr9: 113,316,076-113,317,175 , GRCh37.p13 chr9: 116,078,356-116,079,455 WDR31
    nsv5248410copy number variation1nstd204human GRCh38.p13 chr9: 113,317,576-113,318,675 , GRCh37.p13 chr9: 116,079,856-116,080,955 WDR31
    nsv5139853mobile element insertion1nstd203human GRCh38 chr9: 113,333,283-113,333,293 , GRCh37.p13 chr9: 116,095,563-116,095,573 WDR31
    nsv5139187mobile element insertion1nstd203human GRCh38 chr9: 113,333,284-113,333,293 , GRCh37.p13 chr9: 116,095,564-116,095,573 WDR31
    nsv5137509mobile element insertion1nstd203human GRCh38 chr9: 113,318,232-113,318,248 , GRCh37.p13 chr9: 116,080,512-116,080,528 WDR31
    nsv5137228mobile element insertion1nstd203human GRCh38 chr9: 113,333,278-113,333,293 , GRCh37.p13 chr9: 116,095,558-116,095,573 WDR31
    nsv5132422mobile element insertion1nstd203human GRCh38 chr9: 113,333,289-113,333,293 , GRCh37.p13 chr9: 116,095,569-116,095,573 WDR31
    nsv5131238mobile element insertion1nstd203human GRCh38 chr9: 113,333,273-113,333,293 , GRCh37.p13 chr9: 116,095,553-116,095,573 WDR31
    nsv5130886mobile element insertion1nstd203human GRCh38 chr9: 113,333,281-113,333,293 , GRCh37.p13 chr9: 116,095,561-116,095,573 WDR31
    nsv5129370mobile element insertion1nstd203human GRCh38 chr9: 113,333,279-113,333,289 , GRCh37.p13 chr9: 116,095,559-116,095,569 WDR31
    nsv5125920mobile element insertion1nstd203human GRCh38 chr9: 113,333,285-113,333,293 , GRCh37.p13 chr9: 116,095,565-116,095,573 WDR31
    nsv5124014mobile element insertion1nstd203human GRCh38 chr9: 113,333,280-113,333,293 , GRCh37.p13 chr9: 116,095,560-116,095,573 WDR31
    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