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 215

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978405insertion1nstd209human GRCh38 chr19: 40,625,281-40,625,281 , GRCh37.p13 chr19: 41,131,186-41,131,186 LTBP4
    nsv5708372mobile element insertion1nstd211human GRCh38 chr19: 40,615,213-40,615,213 , GRCh37.p13 chr19: 41,121,119-41,121,119 LTBP4
    nsv5695861mobile element insertion2nstd211human GRCh38 chr19: 40,600,049-40,600,049 , GRCh37.p13 chr19: 41,105,955-41,105,955 LTBP4
    nsv5533310copy number variation1nstd206human GRCh38 chr19: 40,630,269-40,630,390 , GRCh37.p13 chr19: 41,136,174-41,136,295 LTBP4
    nsv5429372mobile element insertion1nstd206human GRCh38 chr19: 40,600,049-40,600,100 , GRCh37.p13 chr19: 41,105,955-41,106,006 LTBP4
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 more genes
    nsv5282305copy number variation1nstd204human GRCh38.p13 chr19: 40,575,051-40,593,471 , GRCh37.p13 chr19: 41,080,957-41,099,377 SPTBN4, LTBP4, 1 more genes
    nsv5175566mobile element insertion1nstd203human GRCh38 chr19: 40,595,910-40,595,920 , GRCh37.p13 chr19: 41,101,816-41,101,826 LTBP4
    nsv5174964mobile element insertion1nstd203human GRCh38 chr19: 40,625,273-40,625,296 , GRCh37.p13 chr19: 41,131,178-41,131,201 LTBP4
    nsv5171711mobile element insertion1nstd203human GRCh38 chr19: 40,630,113-40,630,140 , GRCh37.p13 chr19: 41,136,018-41,136,045 LTBP4
    nsv5028011copy number variation1nstd200human GRCh38 chr19: 40,630,269-40,630,390 , GRCh37.p13 chr19: 41,136,174-41,136,295 LTBP4
    nsv5028010copy number variation1nstd200human GRCh38 chr19: 40,629,511-40,629,673 , GRCh37.p13 chr19: 41,135,416-41,135,578 LTBP4
    nsv5028009copy number variation1nstd200human GRCh38 chr19: 40,600,996-40,603,344 , GRCh37.p13 chr19: 41,106,902-41,109,250 LTBP4
    nsv5028008copy number variation1nstd200human GRCh38 chr19: 40,598,789-40,603,343 , GRCh37.p13 chr19: 41,104,695-41,109,249 LTBP4
    nsv5028007copy number variation1nstd200human GRCh38 chr19: 40,598,790-40,600,924 , GRCh37.p13 chr19: 41,104,696-41,106,830 LTBP4
    nsv5028006copy number variation1nstd200human GRCh38 chr19: 40,587,565-40,591,749 , GRCh37.p13 chr19: 41,093,471-41,097,655 LTBP4, SHKBP1
    nsv5024642copy number variation1nstd200human GRCh38 chr19: 40,622,656-40,641,800 , GRCh37.p13 chr19: 41,128,561-41,147,705 LTBP4
    nsv5024641copy number variation1nstd200human GRCh38 chr19: 40,595,902-40,596,295 , GRCh37.p13 chr19: 41,101,808-41,102,201 LTBP4
    nsv5024640copy number variation1nstd200human GRCh38 chr19: 40,560,179-40,607,043 , GRCh37.p13 chr19: 41,066,085-41,112,949 LTBP4, SPTBN4, 1 more genes
    nsv4868385copy number variation1nstd200human GRCh37 chr19: 41,135,416-41,135,578 , GRCh38.p12 chr19: 40,629,511-40,629,673 LTBP4
    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