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 347

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv6755779copy number variation1nstd229human GRCh38 chr4: 83,035,793-83,042,933 , GRCh37.p13 chr4: 83,956,946-83,964,086 COPS4
    nsv6755397copy number variation1nstd229human GRCh38 chr4: 83,071,201-83,093,900 , GRCh37.p13 chr4: 83,992,354-84,015,053 COPS4, PLAC8
    nsv6754098copy number variation1nstd229human GRCh38 chr4: 83,073,673-83,073,810 , GRCh37.p13 chr4: 83,994,826-83,994,963 COPS4
    nsv6753130copy number variation1nstd229human GRCh38 chr4: 83,063,801-83,069,100 , GRCh37.p13 chr4: 83,984,954-83,990,253 COPS4
    nsv6752620copy number variation1nstd229human GRCh38 chr4: 82,981,801-83,434,800 , GRCh37.p13 chr4: 83,902,954-84,355,953 COPS4, HPSE, 8 more genes
    nsv6752242copy number variation1nstd229human GRCh38 chr4: 82,979,601-83,034,700 , GRCh37.p13 chr4: 83,900,754-83,955,853 LIN54, RNU6-615P, 1 more genes
    nsv6751664copy number variation1nstd229human GRCh38 chr4: 82,990,401-83,187,600 , GRCh37.p13 chr4: 83,911,554-84,108,753 PLAC8, COPS4, 2 more genes
    nsv6751599copy number variation1nstd229human GRCh38 chr4: 83,063,275-83,063,803 , GRCh37.p13 chr4: 83,984,428-83,984,956 COPS4
    nsv6748820copy number variation1nstd229human GRCh38 chr4: 83,052,876-83,059,958 , GRCh37.p13 chr4: 83,974,029-83,981,111 COPS4
    nsv6574536inversion1nstd223human GRCh38 chr4: 83,074,316-83,075,120 , GRCh37.p13 chr4: 83,995,469-83,996,273 COPS4
    nsv6572949inversion1nstd223human GRCh38 chr4: 83,041,510-83,044,419 , GRCh37.p13 chr4: 83,962,663-83,965,572 COPS4
    nsv6572566inversion1nstd223human GRCh38 chr4: 83,047,469-83,048,729 , GRCh37.p13 chr4: 83,968,622-83,969,882 COPS4
    nsv6569092inversion1nstd223human GRCh38 chr4: 83,060,224-83,060,777 , GRCh37.p13 chr4: 83,981,377-83,981,930 COPS4
    nsv6558764inversion1nstd223human GRCh38 chr4: 83,055,666-83,057,749 , GRCh37.p13 chr4: 83,976,819-83,978,902 COPS4
    nsv6395586copy number variation1nstd223human GRCh38 chr4: 83,063,272-83,063,803 , GRCh37.p13 chr4: 83,984,425-83,984,956 COPS4
    nsv6395483copy number variation1nstd223human GRCh38 chr4: 83,032,962-83,034,573 , GRCh37.p13 chr4: 83,954,115-83,955,726 COPS4
    nsv6378538copy number variation1nstd223human GRCh38 chr4: 83,034,048-83,034,601 , GRCh37.p13 chr4: 83,955,201-83,955,754 COPS4
    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