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 585

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068519inversion1nstd229human GRCh38 chr13: 70,633,715-72,604,176 , GRCh37.p13 chr13: 71,207,847-73,178,314 RPL18AP17, LINC00348, 8 more genes
    nsv7061317inversion1nstd229human GRCh38 chr13: 71,095,631-71,509,964 , GRCh37.p13 chr13: 71,669,763-72,084,096 DACH1, RABEPKP1, 1 more genes
    nsv7060146inversion1nstd229human GRCh38 chr13: 70,704,220-75,002,513 , GRCh37.p13 chr13: 71,278,352-75,576,650 RNU4-10P, LOC107987191, 39 more genes
    nsv6957905copy number variation1nstd229human GRCh38 chr13: 70,636,839-71,198,425 , GRCh37.p13 chr13: 71,210,971-71,772,557 LINC00348, MTCL1P1, 1 more genes
    nsv6957497copy number variation1nstd229human GRCh38 chr13: 71,122,327-71,125,566 , GRCh37.p13 chr13: 71,696,459-71,699,698 LINC00348
    nsv6957047copy number variation1nstd229human GRCh38 chr13: 71,054,822-71,058,384 , GRCh37.p13 chr13: 71,628,954-71,632,516 LINC00348
    nsv6955975copy number variation1nstd229human GRCh38 chr13: 71,096,073-71,097,774 , GRCh37.p13 chr13: 71,670,205-71,671,906 LINC00348
    nsv6954555copy number variation1nstd229human GRCh38 chr13: 71,068,178-71,071,017 , GRCh37.p13 chr13: 71,642,310-71,645,149 LINC00348
    nsv6953539copy number variation1nstd229human GRCh38 chr13: 70,643,106-71,429,477 , GRCh37.p13 chr13: 71,217,238-72,003,609 RABEPKP1, LINC00348, 2 more genes
    nsv6953399copy number variation1nstd229human GRCh38 chr13: 71,148,666-71,182,621 , GRCh37.p13 chr13: 71,722,798-71,756,753 LINC00348
    nsv6953278copy number variation1nstd229human GRCh38 chr13: 71,146,401-71,285,800 , GRCh37.p13 chr13: 71,720,533-71,859,932 LINC00348
    nsv6952046copy number variation1nstd229human GRCh38 chr13: 71,057,001-71,062,200 , GRCh37.p13 chr13: 71,631,133-71,636,332 LINC00348
    nsv6951754copy number variation1nstd229human GRCh38 chr13: 71,009,808-71,019,780 , GRCh37.p13 chr13: 71,583,940-71,593,912 LINC00348
    nsv6951715copy number variation1nstd229human GRCh38 chr13: 71,122,860-71,122,937 , GRCh37.p13 chr13: 71,696,992-71,697,069 LINC00348
    nsv6951041copy number variation1nstd229human GRCh38 chr13: 71,135,881-71,136,211 , GRCh37.p13 chr13: 71,710,013-71,710,343 LINC00348
    nsv6950682copy number variation1nstd229human GRCh38 chr13: 71,013,280-71,016,569 , GRCh37.p13 chr13: 71,587,412-71,590,701 LINC00348
    nsv6948917copy number variation1nstd229human GRCh38 chr13: 71,090,715-71,090,928 , GRCh37.p13 chr13: 71,664,847-71,665,060 LINC00348
    nsv6947780copy number variation1nstd229human GRCh38 chr13: 71,056,412-71,063,693 , GRCh37.p13 chr13: 71,630,544-71,637,825 LINC00348
    nsv6947337copy number variation1nstd229human GRCh38 chr13: 71,163,151-71,165,660 , GRCh37.p13 chr13: 71,737,283-71,739,792 LINC00348
    nsv6946676copy number variation1nstd229human GRCh38 chr13: 71,077,615-71,086,315 , GRCh37.p13 chr13: 71,651,747-71,660,447 LINC00348
    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