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 704

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976208inversion1nstd209human GRCh38 chr1: 29,022,566-29,214,534 , GRCh37.p13 chr1: 29,349,078-29,541,046 EPB41, SRSF4, 2 more genes
    nsv5962090insertion1nstd209human GRCh38 chr1: 29,100,313-29,100,313 , GRCh37.p13 chr1: 29,426,825-29,426,825 EPB41
    nsv5957314insertion1nstd209human GRCh38 chr1: 29,055,652-29,055,652 , GRCh37.p13 chr1: 29,382,164-29,382,164 EPB41
    nsv5956479insertion1nstd209human GRCh38 chr1: 29,047,253-29,047,253 , GRCh37.p13 chr1: 29,373,765-29,373,765 EPB41
    nsv5955171insertion1nstd209human GRCh38 chr1: 28,994,950-28,994,950 , GRCh37.p13 chr1: 29,321,462-29,321,462 EPB41
    nsv5886949copy number variation1nstd209human GRCh38 chr1: 28,901,201-28,901,361 , GRCh37.p13 chr1: 29,227,713-29,227,873 EPB41
    nsv5881250copy number variation1nstd209human GRCh38 chr1: 28,994,469-28,994,949 , GRCh37.p13 chr1: 29,320,981-29,321,461 EPB41
    nsv5878876copy number variation1nstd209human GRCh38 chr1: 28,926,002-28,927,943 , GRCh37.p13 chr1: 29,252,514-29,254,455 EPB41
    nsv5878213copy number variation1nstd209human GRCh38 chr1: 28,977,939-28,979,696 , GRCh37.p13 chr1: 29,304,451-29,306,208 EPB41
    nsv5870637copy number variation1nstd209human GRCh38 chr1: 28,988,143-28,992,568 , GRCh37.p13 chr1: 29,314,655-29,319,080 EPB41
    nsv5869796copy number variation1nstd209human GRCh38 chr1: 28,937,468-28,938,605 , GRCh37.p13 chr1: 29,263,980-29,265,117 EPB41
    nsv5829980copy number variation1nstd209human GRCh38 chr1: 29,022,487-29,025,962 , GRCh37.p13 chr1: 29,348,999-29,352,474 EPB41
    nsv5829979copy number variation1nstd209human GRCh38 chr1: 28,925,951-28,928,002 , GRCh37.p13 chr1: 29,252,463-29,254,514 EPB41
    nsv5829829copy number variation1nstd209human GRCh38 chr1: 28,937,510-28,938,609 , GRCh37.p13 chr1: 29,264,022-29,265,121 EPB41
    nsv5829828copy number variation1nstd209human GRCh38 chr1: 28,914,539-28,916,046 , GRCh37.p13 chr1: 29,241,051-29,242,558 EPB41
    nsv5829684copy number variation1nstd209human GRCh38 chr1: 29,043,457-29,044,856 , GRCh37.p13 chr1: 29,369,969-29,371,368 EPB41
    nsv5829683copy number variation1nstd209human GRCh38 chr1: 28,988,110-28,990,668 , GRCh37.p13 chr1: 29,314,622-29,317,180 EPB41
    nsv5829682copy number variation1nstd209human GRCh38 chr1: 28,977,854-28,979,737 , GRCh37.p13 chr1: 29,304,366-29,306,249 EPB41
    nsv5725025mobile element insertion1nstd211human GRCh38 chr1: 28,926,048-28,926,048 , GRCh37.p13 chr1: 29,252,560-29,252,560 EPB41
    nsv5721935mobile element insertion1nstd211human GRCh38 chr1: 29,059,965-29,059,965 , GRCh37.p13 chr1: 29,386,477-29,386,477 EPB41
    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