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 131

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5114576mobile element insertion1nstd203human GRCh38 chr6: 26,286,440-26,286,452 , GRCh37.p13 chr6: 26,286,668-26,286,680 TRX-CAT1-2
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940474copy number variation1nstd200human GRCh38 chr6: 26,236,593-26,320,115 , GRCh37.p13 chr6: 26,236,821-26,320,343 , H2BC10, 17 more genes
    nsv4940473copy number variation1nstd200human GRCh38 chr6: 26,236,594-26,309,109 , GRCh37.p13 chr6: 26,236,822-26,309,337 , TRR-TCG4-1, 11 more genes
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4675352copy number variation1nstd102humanLikely benign GRCh37 chr6: 26,238,509-26,329,714 , GRCh38.p12 chr6: 26,238,281-26,329,486 H3C9P, TRQ-TTG3-2, 22 more genes
    nsv4675256copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,256,525-26,536,884 , GRCh38.p12 chr6: 26,256,297-26,536,656 LOC101928743, TRQ-TTG3-2, 35 more genes
    nsv4598438copy number variation1nstd183human GRCh37 chr6: 26,103,998-26,365,563 , GRCh38.p12 chr6: 26,103,770-26,365,335 , H2AC10P, 46 more genes
    nsv4593441copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,321,490 , GRCh38.p12 chr6: 26,153,056-26,321,262 , H2BC9, 35 more genes
    nsv4521942copy number variation1nstd166human GRCh37.p13 chr6: 26,286,652-26,286,713 , GRCh38.p12 chr6: 26,286,424-26,286,485 TRX-CAT1-2
    nsv4496771mobile element insertion1nstd166human GRCh37.p13 chr6: 26,286,668-26,286,668 , GRCh38.p12 chr6: 26,286,440-26,286,440 TRX-CAT1-2
    nsv4456351copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,896,585-26,287,389 , GRCh38.p12 chr6: 25,896,357-26,287,161 H3P26, H1-6, 44 more genes
    nsv4455820copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,996,066-26,303,969 , GRCh38.p12 chr6: 25,995,838-26,303,741 H4C6, H4C3, 44 more genes
    nsv4455529copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,067,580-26,306,202 , GRCh38.p12 chr6: 26,067,352-26,305,974 RPS10P1, H1-12P, 33 more genes
    nsv4375795copy number variation1nstd173human GRCh37 chr6: 26,207,758-26,303,178 , GRCh38.p12 chr6: 26,207,530-26,302,950 , H1-3, 16 more genes
    nsv4374516copy number variation1nstd173human GRCh37 chr6: 26,128,446-26,856,189 , GRCh38.p12 chr6: 26,128,218-26,888,410 , H3C8, 85 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    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