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 1848

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131012insertion1nstd186human GRCh37 chr13: 108,328,977-108,328,984 , GRCh38.p12 chr13: 107,676,629-107,676,636 NALF1
    nsv6116180mobile element insertion1nstd186human GRCh37 chr13: 108,474,402-108,474,453 , GRCh38.p12 chr13: 107,822,054-107,822,105 NALF1-IT1, NALF1
    nsv5978262insertion1nstd209human GRCh38 chr13: 107,532,197-107,532,197 , GRCh37.p13 chr13: 108,184,545-108,184,545 NALF1
    nsv5976068inversion1nstd209human GRCh38 chr13: 107,321,755-107,323,029 , GRCh37.p13 chr13: 107,974,103-107,975,377 NALF1
    nsv5974690insertion1nstd209human GRCh38 chr13: 107,438,827-107,438,827 , GRCh37.p13 chr13: 108,091,175-108,091,175 NALF1
    nsv5972015insertion1nstd209human GRCh38 chr13: 107,783,266-107,783,266 , GRCh37.p13 chr13: 108,435,614-108,435,614 NALF1
    nsv5967809insertion1nstd209human GRCh38 chr13: 107,822,037-107,822,037 , GRCh37.p13 chr13: 108,474,385-108,474,385 NALF1-IT1, NALF1
    nsv5945981copy number variation1nstd209human GRCh38 chr13: 107,471,192-107,471,289 , GRCh37.p13 chr13: 108,123,540-108,123,637 NALF1
    nsv5945076copy number variation1nstd209human GRCh38 chr13: 107,708,511-107,708,577 , GRCh37.p13 chr13: 108,360,859-108,360,925 NALF1
    nsv5944524copy number variation1nstd209human GRCh38 chr13: 107,494,033-107,494,218 , GRCh37.p13 chr13: 108,146,381-108,146,566 NALF1
    nsv5944472copy number variation1nstd209human GRCh38 chr13: 107,349,571-107,349,670 , GRCh37.p13 chr13: 108,001,919-108,002,018 NALF1
    nsv5939744copy number variation1nstd209human GRCh38 chr13: 107,710,707-107,710,804 , GRCh37.p13 chr13: 108,363,055-108,363,152 NALF1
    nsv5936199copy number variation1nstd209human GRCh38 chr13: 107,653,070-107,653,323 , GRCh37.p13 chr13: 108,305,418-108,305,671 NALF1
    nsv5933624copy number variation1nstd209human GRCh38 chr13: 107,814,772-107,831,153 , GRCh37.p13 chr13: 108,467,120-108,483,501 , NALF1, 1 more genes
    nsv5932511copy number variation1nstd209human GRCh38 chr13: 107,791,696-107,796,237 , GRCh37.p13 chr13: 108,444,044-108,448,585 , NALF1, 1 more genes
    nsv5931323copy number variation1nstd209human GRCh38 chr13: 107,272,190-107,272,512 , GRCh37.p13 chr13: 107,924,538-107,924,860 NALF1
    nsv5931308copy number variation1nstd209human GRCh38 chr13: 107,538,967-107,539,501 , GRCh37.p13 chr13: 108,191,315-108,191,849 NALF1
    nsv5866728copy number variation1nstd209human GRCh38 chr13: 107,814,820-107,828,693 , GRCh37.p13 chr13: 108,467,168-108,481,041 , NALF1, 1 more genes
    nsv5863389copy number variation1nstd209human GRCh38 chr13: 107,791,737-107,794,036 , GRCh37.p13 chr13: 108,444,085-108,446,384 , NALF1-IT1, 1 more genes
    nsv5862631copy number variation1nstd209human GRCh38 chr13: 107,224,654-107,227,971 , GRCh37.p13 chr13: 107,877,002-107,880,319 NALF1
    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