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 219

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925006copy number variation1nstd209human GRCh38 chr11: 77,094,336-77,094,429 , GRCh37.p13 chr11|NW_003871081.1: 95,972-96,065 , GRCh37.p13 chr11: 76,805,382-76,805,475 CAPN5
    nsv5699530mobile element insertion1nstd211human GRCh38 chr11: 77,097,489-77,097,489 , GRCh37.p13 chr11|NW_003871081.1: 99,125-99,125 , GRCh37.p13 chr11: 76,808,535-76,808,535 CAPN5
    nsv5657724insertion1nstd207human GRCh38 chr11: 77,098,728-77,098,728 , GRCh37.p13 chr11|NW_003871081.1: 100,364-100,364 , GRCh37.p13 chr11: 76,809,774-76,809,774 CAPN5
    nsv5652594insertion1nstd207human GRCh38 chr11: 77,098,582-77,098,582 , GRCh37.p13 chr11|NW_003871081.1: 100,218-100,218 , GRCh37.p13 chr11: 76,809,628-76,809,628 CAPN5
    nsv5646176insertion1nstd207human GRCh38 chr11: 77,098,220-77,098,220 , GRCh37.p13 chr11: 76,809,266-76,809,266 , GRCh37.p13 chr11|NW_003871081.1: 99,856-99,856 CAPN5
    nsv5645212insertion1nstd207human GRCh38 chr11: 77,098,068-77,098,068 , GRCh37.p13 chr11: 76,809,114-76,809,114 , GRCh37.p13 chr11|NW_003871081.1: 99,704-99,704 CAPN5
    nsv5587104copy number variation1nstd207human GRCh38 chr11: 77,098,103-77,098,231 , GRCh37.p13 chr11: 76,809,149-76,809,277 , GRCh37.p13 chr11|NW_003871081.1: 99,739-99,867 CAPN5
    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
    nsv4987404copy number variation1nstd200human GRCh38 chr11: 77,105,366-77,108,156 , GRCh37.p13 chr11|NW_003871081.1: 107,002-109,792 , GRCh37.p13 chr11: 76,816,412-76,819,202 CAPN5
    nsv4847218copy number variation1nstd200human GRCh37 chr11: 76,816,412-76,819,202 , GRCh38.p12 chr11: 77,105,366-77,108,156 CAPN5
    nsv4756980insertion1nstd199human GRCh37 chr11: 76,809,056-76,809,056 , GRCh38.p12 chr11: 77,098,010-77,098,010 CAPN5
    nsv4540274insertion1nstd166human GRCh37.p13 chr11: 76,776,816-76,776,816 , GRCh38.p12 chr11: 77,065,769-77,065,769 CAPN5
    nsv4494981mobile element insertion1nstd166human GRCh37.p13 chr11: 76,819,851-76,819,851 , GRCh38.p12 chr11: 77,108,805-77,108,805 CAPN5
    nsv4489711mobile element insertion1nstd166human GRCh37.p13 chr11: 76,829,367-76,829,367 , GRCh38.p12 chr11: 77,118,321-77,118,321 CAPN5
    nsv4485465mobile element insertion1nstd166human GRCh37.p13 chr11: 76,798,583-76,798,583 , GRCh38.p12 chr11: 77,087,537-77,087,537 CAPN5
    nsv4478552mobile element insertion1nstd166human GRCh37.p13 chr11: 76,792,286-76,792,286 , GRCh38.p12 chr11: 77,081,240-77,081,240 CAPN5
    nsv4446434insertion1nstd175human GRCh37 chr11: 76,809,107-76,809,107 , GRCh38.p12 chr11: 77,098,061-77,098,061 CAPN5
    nsv4210732copy number variation1nstd166human GRCh37.p13 chr11: 76,785,296-76,794,307 , GRCh38.p12 chr11: 77,074,250-77,083,261 CAPN5
    nsv4206200copy number variation1nstd166human GRCh37.p13 chr11: 76,811,957-76,812,251 , GRCh38.p12 chr11: 77,100,911-77,101,205 OMP, CAPN5
    nsv4201116copy number variation1nstd166human GRCh37.p13 chr11: 76,731,715-76,825,853 , GRCh38.p12 chr11: 77,020,671-77,114,807 CAPN5, OMP, 4 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