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 1046

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7140657copy number variation1nstd232human GRCh37.p13 chr7: 156,313,041-156,313,156 , GRCh38.p12 chr7: 156,520,347-156,520,462 RNF32-DT
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7059328inversion1nstd229human GRCh38 chr7: 156,594,383-156,594,524 , GRCh37.p13 chr7: 156,387,077-156,387,218 RNF32-DT
    nsv6837836copy number variation1nstd229human GRCh38 chr7: 156,537,362-156,546,003 , GRCh37.p13 chr7: 156,330,056-156,338,697 LINC00244, RNF32-DT
    nsv6835563copy number variation1nstd229human GRCh38 chr7: 156,504,001-156,521,200 , GRCh37.p13 chr7: 156,296,695-156,313,894 RNF32-DT, LOC112268012
    nsv6835358copy number variation1nstd229human GRCh38 chr7: 156,506,101-156,522,400 , GRCh37.p13 chr7: 156,298,795-156,315,094 LOC112268012, RNF32-DT
    nsv6835157copy number variation1nstd229human GRCh38 chr7: 155,586,961-156,721,504 , GRCh37.p13 chr7: 155,379,656-156,514,198 LOC105375597, RBM33, 15 more genes
    nsv6834826copy number variation1nstd229human GRCh38 chr7: 156,531,943-156,542,827 , GRCh37.p13 chr7: 156,324,637-156,335,521 RNF32-DT, LINC00244
    nsv6832632copy number variation1nstd229human GRCh38 chr7: 156,630,172-156,631,810 , GRCh37.p13 chr7: 156,422,866-156,424,504 RPL26P23, RNF32-DT
    nsv6832434copy number variation1nstd229human GRCh38 chr7: 156,498,112-156,498,218 , GRCh37.p13 chr7: 156,290,806-156,290,912 RNF32-DT
    nsv6832043copy number variation1nstd229human GRCh38 chr7: 156,640,776-156,651,066 , GRCh37.p13 chr7: 156,433,470-156,443,760 RNF32-DT, RNF32
    nsv6831773copy number variation1nstd229human GRCh38 chr7: 156,622,023-156,622,231 , GRCh37.p13 chr7: 156,414,717-156,414,925 RNF32-DT
    nsv6831746copy number variation1nstd229human GRCh38 chr7: 156,504,201-156,521,300 , GRCh37.p13 chr7: 156,296,895-156,313,994 LOC112268012, RNF32-DT
    nsv6831041copy number variation1nstd229human GRCh38 chr7: 156,617,931-156,627,633 , GRCh37.p13 chr7: 156,410,625-156,420,327 RNF32-DT
    nsv6830907copy number variation1nstd229human GRCh38 chr7: 156,553,736-156,554,026 , GRCh37.p13 chr7: 156,346,430-156,346,720 RNF32-DT
    nsv6830264copy number variation1nstd229human GRCh38 chr7: 156,522,913-156,529,153 , GRCh37.p13 chr7: 156,315,607-156,321,847 RNF32-DT, LOC112268012
    nsv6829602copy number variation1nstd229human GRCh38 chr7: 156,470,225-156,475,892 , GRCh37.p13 chr7: 156,262,919-156,268,586 RNF32-DT
    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