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 363

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049124inversion1nstd229human GRCh38 chr2: 174,401,435-175,981,960 , GRCh37.p13 chr2: 175,266,163-176,846,688 LNPK, RNU7-44P, 19 more genes
    nsv7046180inversion1nstd229human GRCh38 chr2: 175,161,314-175,161,425 , GRCh37.p13 chr2: 176,026,042-176,026,153 ATF2
    nsv7041531inversion1nstd229human GRCh38 chr2: 175,072,891-175,125,235 , GRCh37.p13 chr2: 175,937,619-175,989,963 ATF2
    nsv6695637copy number variation1nstd229human GRCh38 chr2: 175,145,396-175,148,926 , GRCh37.p13 chr2: 176,010,124-176,013,654 ATF2
    nsv6694525copy number variation1nstd229human GRCh38 chr2: 175,096,721-175,101,235 , GRCh37.p13 chr2: 175,961,449-175,965,963 ATF2
    nsv6689068copy number variation1nstd229human GRCh38 chr2: 175,082,901-175,084,600 , GRCh37.p13 chr2: 175,947,629-175,949,328 ATF2
    nsv6686077copy number variation1nstd229human GRCh38 chr2: 175,094,492-175,094,647 , GRCh37.p13 chr2: 175,959,220-175,959,375 ATF2
    nsv6685454copy number variation1nstd229human GRCh38 chr2: 175,144,449-175,148,149 , GRCh37.p13 chr2: 176,009,177-176,012,877 ATF2
    nsv6685355copy number variation1nstd229human GRCh38 chr2: 175,149,018-175,154,425 , GRCh37.p13 chr2: 176,013,746-176,019,153 ATF2
    nsv6685285copy number variation1nstd229human GRCh38 chr2: 175,156,001-175,206,700 , GRCh37.p13 chr2: 176,020,729-176,071,428 MIR933, ATP5MC3, 2 more genes
    nsv6684605copy number variation1nstd229human GRCh38 chr2: 175,161,022-175,163,224 , GRCh37.p13 chr2: 176,025,750-176,027,952 ATF2
    nsv6683505copy number variation1nstd229human GRCh38 chr2: 175,109,209-175,109,286 , GRCh37.p13 chr2: 175,973,937-175,974,014 ATF2
    nsv6682885copy number variation1nstd229human GRCh38 chr2: 175,125,410-175,128,491 , GRCh37.p13 chr2: 175,990,138-175,993,219 ATF2
    nsv6679376copy number variation1nstd229human GRCh38 chr2: 175,146,211-175,146,288 , GRCh37.p13 chr2: 176,010,939-176,011,016 ATF2
    nsv6678957copy number variation1nstd229human GRCh38 chr2: 175,080,722-175,081,495 , GRCh37.p13 chr2: 175,945,450-175,946,223 ATF2
    nsv6637115copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,143,352-180,999,636 , GRCh38.p12 chr2: 174,278,624-180,134,909 RNU6-5P, LOC101927073, 107 more genes
    nsv6554426inversion1nstd223human GRCh38 chr2: 175,094,122-175,095,110 , GRCh37.p13 chr2: 175,958,850-175,959,838 ATF2
    nsv6550321inversion1nstd223human GRCh38 chr2: 175,163,919-175,164,871 , GRCh37.p13 chr2: 176,028,647-176,029,599 ATF2
    nsv6542353inversion1nstd223human GRCh38 chr2: 175,110,301-175,110,599 , GRCh37.p13 chr2: 175,975,029-175,975,327 ATF2
    nsv6353124copy number variation1nstd223human GRCh38 chr2: 175,120,946-175,121,514 , GRCh37.p13 chr2: 175,985,674-175,986,242 ATF2
    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