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 265

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138853insertion1nstd232human GRCh37.p13 chr6: 112,562,337-112,562,337 , GRCh38.p12 chr6: 112,241,136-112,241,136 LAMA4, LAMA4-AS1
    nsv7053450inversion1nstd229human GRCh38 chr6: 112,228,366-112,286,553 , GRCh37.p13 chr6|NW_003871062.1: 225,887-262,912 , GRCh37.p13 chr6: 112,549,567-112,586,593 LAMA4, LOC107986632, 1 more genes
    nsv7048821inversion1nstd229human GRCh38 chr6: 112,221,453-112,351,413 , GRCh37.p13 chr6: 112,586,594-112,672,615 LAMA4, LAMA4-AS1, 3 more genes
    nsv7046333inversion1nstd229human GRCh38 chr6: 112,252,766-112,256,689 , GRCh37.p13 chr6|NW_003871062.1: 250,287-254,210 , GRCh37.p13 chr6: 112,573,968-112,577,891 LAMA4, LAMA4-AS1
    nsv7040174inversion1nstd229human GRCh38 chr6: 112,249,822-112,256,984 , GRCh37.p13 chr6|NW_003871062.1: 247,343-254,505 , GRCh37.p13 chr6: 112,571,024-112,578,186 LAMA4-AS1, LAMA4
    nsv6818040copy number variation1nstd229human GRCh38 chr6: 112,252,079-112,252,295 , GRCh37.p13 chr6: 112,573,281-112,573,497 , GRCh37.p13 chr6|NW_003871062.1: 249,600-249,816 LAMA4, LAMA4-AS1
    nsv6816302copy number variation1nstd229human GRCh38 chr6: 112,234,077-112,251,232 , GRCh37.p13 chr6|NW_003871062.1: 231,598-248,753 , GRCh37.p13 chr6: 112,555,278-112,572,434 LAMA4, LAMA4-AS1
    nsv6815593copy number variation1nstd229human GRCh38 chr6: 112,221,401-112,366,500 , GRCh37.p13 chr6: 112,586,594-112,687,702 RPSAP45, LAMA4-AS1, 6 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6814649copy number variation1nstd229human GRCh38 chr6: 112,279,104-112,286,523 , GRCh37.p13 chr6: 112,600,306-112,607,725 LOC107986632, LAMA4-AS1
    nsv6808847copy number variation1nstd229human GRCh38 chr6: 112,305,988-112,321,353 , GRCh37.p13 chr6: 112,627,190-112,642,555 LAMA4-AS1
    nsv6806048copy number variation1nstd229human GRCh38 chr6: 112,248,444-112,318,919 , GRCh37.p13 chr6: 112,586,594-112,640,121 LOC107986632, LAMA4, 1 more genes
    nsv6804600copy number variation1nstd229human GRCh38 chr6: 112,133,360-112,235,910 , GRCh37.p13 chr6: 112,454,562-112,557,111 , GRCh37.p13 chr6|NW_003871062.1: 130,881-233,431 LAMA4-AS1, LOC107986633, 2 more genes
    nsv6804045copy number variation1nstd229human GRCh38 chr6: 112,258,995-112,328,294 , GRCh37.p13 chr6: 112,586,594-112,649,496 LAMA4-AS1, LOC100128588, 1 more genes
    nsv6803993copy number variation1nstd229human GRCh38 chr6: 112,288,736-112,301,766 , GRCh37.p13 chr6: 112,609,938-112,622,968 LAMA4-AS1, LOC107986632
    nsv6801765copy number variation1nstd229human GRCh38 chr6: 112,303,420-112,315,994 , GRCh37.p13 chr6: 112,624,622-112,637,196 LAMA4-AS1
    nsv6800168copy number variation1nstd229human GRCh38 chr6: 112,243,115-112,243,194 , GRCh37.p13 chr6: 112,564,317-112,564,396 , GRCh37.p13 chr6|NW_003871062.1: 240,636-240,715 LAMA4-AS1, LAMA4
    nsv6630654copy number variation2nstd224human GRCh37 chr6: 112,615,438-113,544,965 , GRCh38.p12 chr6: 112,294,236-113,223,763 KRT18P65, LOC100128588, 19 more genes
    nsv6615065copy number variation1nstd223human GRCh38 chr6: 112,291,457-113,231,778 , GRCh37.p13 chr6: 112,612,659-113,552,980 KRT18P65, LOC105377949, 19 more genes
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    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