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 95

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919708copy number variation1nstd209human GRCh38 chr11: 61,438,937-61,440,197 , GRCh37.p13 chr11: 61,206,409-61,207,669 SDHAF2
    nsv5850067copy number variation1nstd209human GRCh38 chr11: 61,438,889-61,440,188 , GRCh37.p13 chr11: 61,206,361-61,207,660 SDHAF2
    nsv5703169mobile element insertion2nstd211human GRCh38 chr11: 61,434,610-61,434,610 , GRCh37.p13 chr11: 61,202,082-61,202,082 SDHAF2
    nsv5497652copy number variation1nstd206human GRCh38 chr11: 61,435,852-61,458,485 , GRCh37.p13 chr11: 61,203,324-61,225,957 SDHAF2, RN7SL23P
    nsv5495770copy number variation1nstd206human GRCh38 chr11: 61,438,921-61,440,247 , GRCh37.p13 chr11: 61,206,393-61,207,719 SDHAF2
    nsv5380887copy number variation1nstd102humanUncertain significance GRCh37 chr11: 61,197,619-61,213,543 , GRCh38.p12 chr11: 61,430,147-61,446,071 CPSF7, SDHAF2, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4979650copy number variation1nstd200human GRCh38 chr11: 61,438,963-61,440,198 , GRCh37.p13 chr11: 61,206,435-61,207,670 SDHAF2
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4842468copy number variation1nstd200human GRCh37 chr11: 61,206,435-61,207,670 , GRCh38.p12 chr11: 61,438,963-61,440,198 SDHAF2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4683810copy number variation2nstd102humanUncertain significance, Likely pathogenic GRCh37 chr11: 61,205,087-61,213,543 , GRCh38.p12 chr11: 61,437,615-61,446,071 SDHAF2, RN7SL23P
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4490230mobile element insertion1nstd166human GRCh37.p13 chr11: 61,200,159-61,200,159 , GRCh38.p12 chr11: 61,432,687-61,432,687 SDHAF2
    nsv4457060copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,499,486-61,529,578 , GRCh38.p12 chr11: 60,732,013-61,762,106 TMEM109, LOC101927495, 41 more genes
    nsv4454580copy number variation1nstd102humanUncertain significance GRCh38 chr11: 61,437,615-61,446,081 , GRCh37 chr11: 61,205,087-61,213,553 SDHAF2, RN7SL23P
    nsv3915850copy number variation1nstd102humanLikely benign GRCh37 chr11: 61,177,001-61,588,631 , GRCh38 chr11: 61,409,529-61,821,159 , NCBI36 chr11: 60,933,577-61,345,207 TMEM258, RN7SL23P, 18 more genes
    nsv3912748copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,948,809-61,284,302 , NCBI36 chr11: 60,705,385-61,040,878 , GRCh38 chr11: 61,181,337-61,516,830 DDB1, LOC105369329, 15 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