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 292

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964266insertion1nstd209human GRCh38 chr4: 42,326,680-42,326,680 , GRCh37.p13 chr4: 42,328,697-42,328,697 LOC105374428
    nsv5904080copy number variation1nstd209human GRCh38 chr4: 42,369,658-42,370,329 , GRCh37.p13 chr4: 42,371,675-42,372,346 LOC105374428
    nsv5895766copy number variation1nstd209human GRCh38 chr4: 42,358,440-42,359,260 , GRCh37.p13 chr4: 42,360,457-42,361,277 LOC105374428
    nsv5615441insertion1nstd207human GRCh38 chr4: 42,326,676-42,326,676 , GRCh37.p13 chr4: 42,328,693-42,328,693 LOC105374428
    nsv5607012insertion1nstd207human GRCh38 chr4: 42,300,179-42,300,179 , GRCh37.p13 chr4: 42,302,196-42,302,196 LOC105374428
    nsv5534523insertion1nstd206human GRCh38 chr4: 42,326,698-42,326,730 , GRCh37.p13 chr4: 42,328,715-42,328,747 LOC105374428
    nsv5469450copy number variation1nstd206human GRCh38 chr4: 42,358,440-42,359,266 , GRCh37.p13 chr4: 42,360,457-42,361,283 LOC105374428
    nsv5457104copy number variation1nstd206human GRCh38 chr4: 42,324,014-42,327,640 , GRCh37.p13 chr4: 42,326,031-42,329,657 LOC105374428
    nsv5455698copy number variation1nstd206human GRCh38 chr4: 42,369,658-42,370,332 , GRCh37.p13 chr4: 42,371,675-42,372,349 LOC105374428
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4928529copy number variation1nstd200human GRCh38 chr4: 42,370,430-42,374,962 , GRCh37.p13 chr4: 42,372,447-42,376,979 LOC105374428
    nsv4928528copy number variation1nstd200human GRCh38 chr4: 42,325,095-42,334,539 , GRCh37.p13 chr4: 42,327,112-42,336,556 LOC105374428
    nsv4928527copy number variation1nstd200human GRCh38 chr4: 42,303,678-42,304,639 , GRCh37.p13 chr4: 42,305,695-42,306,656 LOC105374428
    nsv4925544copy number variation1nstd200human GRCh38 chr4: 42,243,347-42,303,144 , GRCh37.p13 chr4: 42,245,364-42,305,161 LOC105374428
    nsv4791583copy number variation1nstd200human GRCh37 chr4: 42,372,447-42,376,979 , GRCh38.p12 chr4: 42,370,430-42,374,962 LOC105374428
    nsv4791582copy number variation1nstd200human GRCh37 chr4: 42,371,675-42,372,349 , GRCh38.p12 chr4: 42,369,658-42,370,332 LOC105374428
    nsv4791581copy number variation1nstd200human GRCh37 chr4: 42,305,695-42,306,656 , GRCh38.p12 chr4: 42,303,678-42,304,639 LOC105374428
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 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