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 772

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054823inversion1nstd229human GRCh38 chr6: 143,170,072-148,803,855 , GRCh37.p13 chr6: 143,491,209-149,124,991 FBXO30, C4orf46P4, 56 more genes
    nsv7053992inversion1nstd229human GRCh38 chr6: 146,320,514-146,325,361 , GRCh37.p13 chr6: 146,641,650-146,646,497 GRM1
    nsv7053654inversion1nstd229human GRCh38 chr6: 143,517,092-147,615,699 , GRCh37.p13 chr6: 143,838,229-147,936,835 PHACTR2, LOC105378040, 37 more genes
    nsv7053509inversion1nstd229human GRCh38 chr6: 146,401,822-146,401,842 , GRCh37.p13 chr6: 146,722,958-146,722,978 GRM1
    nsv7053302inversion1nstd229human GRCh38 chr6: 146,090,970-146,096,802 , GRCh37.p13 chr6: 146,412,106-146,417,938 GRM1
    nsv7053270inversion1nstd229human GRCh38 chr6: 146,284,665-146,288,681 , GRCh37.p13 chr6: 146,605,801-146,609,817 GRM1
    nsv7050103inversion1nstd229human GRCh38 chr6: 146,036,146-146,038,586 , GRCh37.p13 chr6: 146,357,282-146,359,722 GRM1
    nsv7045988inversion1nstd229human GRCh38 chr6: 146,316,068-146,325,668 , GRCh37.p13 chr6: 146,637,204-146,646,804 GRM1
    nsv7045534inversion1nstd229human GRCh38 chr6: 146,356,235-146,364,961 , GRCh37.p13 chr6: 146,677,371-146,686,097 GRM1
    nsv7045355inversion1nstd229human GRCh38 chr6: 146,434,524-146,434,553 , GRCh37.p13 chr6: 146,755,660-146,755,689 GRM1
    nsv7042532inversion1nstd229human GRCh38 chr6: 146,282,641-146,288,910 , GRCh37.p13 chr6: 146,603,777-146,610,046 GRM1
    nsv7040321inversion1nstd229human GRCh38 chr6: 146,014,527-146,095,562 , GRCh37.p13 chr6: 146,335,663-146,416,698 GRM1
    nsv6817610copy number variation1nstd229human GRCh38 chr6: 146,074,852-146,075,299 , GRCh37.p13 chr6: 146,395,988-146,396,435 GRM1
    nsv6817228copy number variation1nstd229human GRCh38 chr6: 146,160,193-146,164,860 , GRCh37.p13 chr6: 146,481,329-146,485,996 GRM1
    nsv6817190copy number variation1nstd229human GRCh38 chr6: 146,169,942-146,196,235 , GRCh37.p13 chr6: 146,491,078-146,517,371 FUNDC2P3, GRM1
    nsv6817063copy number variation1nstd229human GRCh38 chr6: 146,181,259-146,186,507 , GRCh37.p13 chr6: 146,502,395-146,507,643 GRM1
    nsv6816189copy number variation1nstd229human GRCh38 chr6: 146,370,900-146,378,120 , GRCh37.p13 chr6: 146,692,036-146,699,256 GRM1
    nsv6816041copy number variation1nstd229human GRCh38 chr6: 146,398,056-146,398,222 , GRCh37.p13 chr6: 146,719,192-146,719,358 GRM1
    nsv6814538copy number variation1nstd229human GRCh38 chr6: 146,106,887-146,111,047 , GRCh37.p13 chr6: 146,428,023-146,432,183 GRM1
    nsv6814409copy number variation1nstd229human GRCh38 chr6: 146,269,053-146,276,988 , GRCh37.p13 chr6: 146,590,189-146,598,124 GRM1
    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