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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959258insertion1nstd209human GRCh38 chr6: 116,577,507-116,577,507 , GRCh37.p13 chr6: 116,898,670-116,898,670 RWDD1
    nsv5686961mobile element insertion2nstd211human GRCh38 chr6: 116,577,523-116,577,523 , GRCh37.p13 chr6: 116,898,686-116,898,686 RWDD1
    nsv5635714insertion1nstd207human GRCh38 chr6: 116,577,507-116,577,507 , GRCh37.p13 chr6: 116,898,670-116,898,670 RWDD1
    nsv5403148mobile element insertion1nstd206human GRCh38 chr6: 116,577,507-116,577,507 , GRCh37.p13 chr6: 116,898,670-116,898,670 RWDD1
    nsv5119530mobile element insertion1nstd203human GRCh38 chr6: 116,585,223-116,585,238 , GRCh37.p13 chr6: 116,906,386-116,906,401 RWDD1
    nsv5117921mobile element insertion1nstd203human GRCh38 chr6: 116,577,506-116,577,523 , GRCh37.p13 chr6: 116,898,669-116,898,686 RWDD1
    nsv5112506mobile element insertion1nstd203human GRCh38 chr6: 116,577,513-116,577,523 , GRCh37.p13 chr6: 116,898,676-116,898,686 RWDD1
    nsv5109756mobile element insertion1nstd203human GRCh38 chr6: 116,577,507-116,577,523 , GRCh37.p13 chr6: 116,898,670-116,898,686 RWDD1
    nsv5108716mobile element insertion1nstd203human GRCh38 chr6: 116,577,514-116,577,523 , GRCh37.p13 chr6: 116,898,677-116,898,686 RWDD1
    nsv5104644mobile element insertion1nstd203human GRCh38 chr6: 116,577,505-116,577,523 , GRCh37.p13 chr6: 116,898,668-116,898,686 RWDD1
    nsv5104385mobile element insertion1nstd203human GRCh38 chr6: 116,577,523-116,577,523 , GRCh37.p13 chr6: 116,898,686-116,898,686 RWDD1
    nsv5102445mobile element insertion1nstd203human GRCh38 chr6: 116,577,512-116,577,522 , GRCh37.p13 chr6: 116,898,675-116,898,685 RWDD1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945592copy number variation1nstd200human GRCh38 chr6: 116,586,080-116,597,208 , GRCh37.p13 chr6: 116,907,243-116,918,371 RSPH4A, RWDD1
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
    nsv4755544insertion1nstd199human GRCh37 chr6: 116,898,681-116,898,681 , GRCh38.p12 chr6: 116,577,518-116,577,518 RWDD1
    nsv4724557insertion1nstd186human GRCh37 chr6: 116,898,670-116,898,670 , GRCh38.p12 chr6: 116,577,507-116,577,507 RWDD1
    nsv4686641mobile element insertion1nstd186human GRCh37 chr6: 116,898,686-116,898,686 , GRCh38.p12 chr6: 116,577,523-116,577,523 RWDD1
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4546015insertion1nstd166human GRCh37.p13 chr6: 116,898,670-116,898,670 , GRCh38.p12 chr6: 116,577,507-116,577,507 RWDD1
    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