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 143

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7073083inversion1nstd229human GRCh38 chr11: 59,669,249-59,699,930 , GRCh37.p13 chr11: 59,436,722-59,467,403 PATL1-DT, PATL1
    nsv6916571copy number variation1nstd229human GRCh38 chr11: 59,653,876-59,654,375 , GRCh37.p13 chr11: 59,421,349-59,421,848 PATL1
    nsv6912932copy number variation1nstd229human GRCh38 chr11: 59,667,485-59,675,307 , GRCh37.p13 chr11: 59,434,958-59,442,780 PATL1, PATL1-DT
    nsv6912249copy number variation1nstd229human GRCh38 chr11: 59,664,501-59,683,700 , GRCh37.p13 chr11: 59,431,974-59,451,173 PATL1, PATL1-DT
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6592020inversion1nstd223human GRCh38 chr11: 59,657,917-59,658,610 , GRCh37.p13 chr11: 59,425,390-59,426,083 PATL1
    nsv6472573copy number variation1nstd223human GRCh38 chr11: 59,643,679-59,646,812 , GRCh37.p13 chr11: 59,411,152-59,414,285 PATL1
    nsv6464542copy number variation1nstd223human GRCh38 chr11: 59,640,446-59,640,759 , GRCh37.p13 chr11: 59,407,919-59,408,232 PATL1
    nsv6463854copy number variation1nstd223human GRCh38 chr11: 59,668,401-59,670,100 , GRCh37.p13 chr11: 59,435,874-59,437,573 PATL1
    nsv6463126copy number variation1nstd223human GRCh38 chr11: 59,664,401-59,672,300 , GRCh37.p13 chr11: 59,431,874-59,439,773 PATL1, PATL1-DT
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6091806insertion1nstd212human GRCh38 chr11: 59,636,010-59,636,010 , GRCh37.p13 chr11: 59,403,483-59,403,483 PATL1, LOC101927226
    nsv6081378insertion1nstd212human GRCh38 chr11: 59,645,351-59,645,351 , GRCh37.p13 chr11: 59,412,824-59,412,824 PATL1
    nsv5975297insertion1nstd209human GRCh38 chr11: 59,636,010-59,636,010 , GRCh37.p13 chr11: 59,403,483-59,403,483 PATL1, LOC101927226
    nsv5968538insertion1nstd209human GRCh38 chr11: 59,652,064-59,652,064 , GRCh37.p13 chr11: 59,419,537-59,419,537 PATL1
    nsv5921819copy number variation1nstd209human GRCh38 chr11: 59,640,446-59,640,758 , GRCh37.p13 chr11: 59,407,919-59,408,231 PATL1
    nsv5658578insertion1nstd207human GRCh38 chr11: 59,645,321-59,645,321 , GRCh37.p13 chr11: 59,412,794-59,412,794 PATL1
    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