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 739

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144768insertion1nstd232human GRCh37.p13 chr7: 102,573,009-102,573,009 , GRCh38.p12 chr7: 102,932,562-102,932,562 LRRC17, FBXL13
    nsv7137855insertion1nstd232human GRCh37.p13 chr7: 102,488,720-102,488,720 , GRCh38.p12 chr7: 102,848,273-102,848,273 FAM185A, FBXL13
    nsv7056653inversion1nstd229human GRCh38 chr7: 102,980,451-102,995,144 , GRCh37.p13 chr7: 102,620,898-102,635,591 FBXL13
    nsv7053206inversion1nstd229human GRCh38 chr7: 102,987,091-102,990,485 , GRCh37.p13 chr7: 102,627,538-102,630,932 FBXL13
    nsv7052662inversion1nstd229human GRCh38 chr7: 102,309,147-103,483,817 , GRCh37.p13 chr7: 102,072,448-103,124,264 S100A11P1, RPL7AP39, 46 more genes
    nsv7050836inversion1nstd229human GRCh38 chr7: 103,069,449-103,073,058 , GRCh37.p13 chr7: 102,709,896-102,713,505 ARMC10, FBXL13
    nsv7048083inversion1nstd229human GRCh38 chr7: 102,988,365-102,988,774 , GRCh37.p13 chr7: 102,628,812-102,629,221 FBXL13
    nsv7048035inversion1nstd229human GRCh38 chr7: 102,985,316-102,990,801 , GRCh37.p13 chr7: 102,625,763-102,631,248 FBXL13
    nsv7046426inversion1nstd229human GRCh38 chr7: 102,987,098-102,994,965 , GRCh37.p13 chr7: 102,627,545-102,635,412 FBXL13
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv7038233inversion1nstd229human GRCh38 chr7: 102,692,053-102,833,999 , GRCh37.p13 chr7: 102,332,500-102,474,446 FAM185A, RPL7AP39, 4 more genes
    nsv6837745copy number variation1nstd229human GRCh38 chr7: 102,818,582-102,859,895 , GRCh37.p13 chr7: 102,459,029-102,500,342 RNU6-1136P, FAM185A, 2 more genes
    nsv6837723copy number variation1nstd229human GRCh38 chr7: 102,930,705-102,932,050 , GRCh37.p13 chr7: 102,571,152-102,572,497 LRRC17, FBXL13
    nsv6837492copy number variation1nstd229human GRCh38 chr7: 102,980,788-102,984,203 , GRCh37.p13 chr7: 102,621,235-102,624,650 FBXL13
    nsv6837481copy number variation1nstd229human GRCh38 chr7: 102,980,801-102,983,200 , GRCh37.p13 chr7: 102,621,248-102,623,647 FBXL13
    nsv6835745copy number variation1nstd229human GRCh38 chr7: 102,892,570-102,898,429 , GRCh37.p13 chr7: 102,533,017-102,538,876 FBXL13
    nsv6834190copy number variation1nstd229human GRCh38 chr7: 102,957,501-102,962,800 , GRCh37.p13 chr7: 102,597,948-102,603,247 FBXL13
    nsv6832114copy number variation1nstd229human GRCh38 chr7: 102,874,516-102,881,552 , GRCh37.p13 chr7: 102,514,963-102,521,999 FBXL13
    nsv6831771copy number variation1nstd229human GRCh38 chr7: 102,917,932-102,924,325 , GRCh37.p13 chr7: 102,558,379-102,564,772 LRRC17, FBXL13
    nsv6831579copy number variation1nstd229human GRCh38 chr7: 103,024,170-103,024,187 , GRCh37.p13 chr7: 102,664,617-102,664,634 FBXL13
    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