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 338

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057352inversion1nstd229human GRCh38 chr2: 223,759,278-223,759,328 , GRCh37.p13 chr2: 224,623,995-224,624,045 AP1S3
    nsv7055926inversion1nstd229human GRCh38 chr2: 223,723,053-227,096,551 , GRCh37.p13 chr2: 224,587,770-227,961,267 CUL3, MRPL44, 23 more genes
    nsv7054862inversion1nstd229human GRCh38 chr2: 223,800,886-223,804,351 , GRCh37.p13 chr2: 224,665,603-224,669,068 AP1S3
    nsv7047506inversion1nstd229human GRCh38 chr2: 222,618,340-223,958,759 , GRCh37.p13 chr2: 223,483,059-224,823,476 LOC105373903, LOC105373906, 22 more genes
    nsv7047209inversion1nstd229human GRCh38 chr2: 222,803,564-227,992,948 , GRCh37.p13 chr2: 223,668,283-228,857,664 MFF, LOC100289117, 55 more genes
    nsv7043640inversion1nstd229human GRCh38 chr2: 222,841,128-228,011,478 , GRCh37.p13 chr2: 223,705,846-228,876,194 MFF-DT, LOC105373905, 55 more genes
    nsv6698076copy number variation1nstd229human GRCh38 chr2: 223,817,991-223,822,071 , GRCh37.p13 chr2: 224,682,708-224,686,788 AP1S3
    nsv6698014copy number variation1nstd229human GRCh38 chr2: 223,821,101-223,846,300 , GRCh37.p13 chr2: 224,685,818-224,711,017 AP1S3
    nsv6694318copy number variation1nstd229human GRCh38 chr2: 223,700,901-223,846,300 , GRCh37.p13 chr2: 224,565,618-224,711,017 AP1S3, MLXP1
    nsv6693492copy number variation1nstd229human GRCh38 chr2: 223,751,807-223,774,146 , GRCh37.p13 chr2: 224,616,524-224,638,863 AP1S3
    nsv6690691copy number variation1nstd229human GRCh38 chr2: 223,754,319-223,754,874 , GRCh37.p13 chr2: 224,619,036-224,619,591 AP1S3
    nsv6689860copy number variation1nstd229human GRCh38 chr2: 223,778,176-223,778,194 , GRCh37.p13 chr2: 224,642,893-224,642,911 AP1S3
    nsv6687541copy number variation1nstd229human GRCh38 chr2: 223,771,708-223,778,810 , GRCh37.p13 chr2: 224,636,425-224,643,527 AP1S3
    nsv6686518copy number variation1nstd229human GRCh38 chr2: 223,802,873-223,835,640 , GRCh37.p13 chr2: 224,667,590-224,700,357 AP1S3
    nsv6684135copy number variation1nstd229human GRCh38 chr2: 223,759,083-223,761,554 , GRCh37.p13 chr2: 224,623,800-224,626,271 AP1S3
    nsv6682951copy number variation1nstd229human GRCh38 chr2: 223,792,757-223,797,124 , GRCh37.p13 chr2: 224,657,474-224,661,841 AP1S3
    nsv6682260copy number variation1nstd229human GRCh38 chr2: 223,801,298-223,805,942 , GRCh37.p13 chr2: 224,666,015-224,670,659 AP1S3
    nsv6682259copy number variation1nstd229human GRCh38 chr2: 223,817,520-223,818,124 , GRCh37.p13 chr2: 224,682,237-224,682,841 AP1S3
    nsv6682106copy number variation1nstd229human GRCh38 chr2: 223,796,152-223,889,591 , GRCh37.p13 chr2: 224,660,869-224,754,308 WDFY1, AP1S3
    nsv6680849copy number variation1nstd229human GRCh38 chr2: 223,777,166-223,779,273 , GRCh37.p13 chr2: 224,641,883-224,643,990 AP1S3
    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