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 427

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7096595copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 191,835,429-192,012,929 , GRCh38.p12 chr2: 190,970,703-191,148,203 STAT1, STAT4, 4 more genes
    nsv7096119copy number variation2nstd102humanUncertain significance GRCh37 chr2: 189,839,216-192,012,929 , GRCh38.p12 chr2: 188,974,490-191,148,203 NAB1, ANKAR, 38 more genes
    nsv7049599inversion1nstd229human GRCh38 chr2: 191,116,490-191,116,540 , GRCh37.p13 chr2: 191,981,216-191,981,266 STAT4
    nsv7042155inversion1nstd229human GRCh38 chr2: 191,150,217-191,150,269 , GRCh37.p13 chr2: 192,014,943-192,014,995 STAT4
    nsv7039635inversion1nstd229human GRCh38 chr2: 191,160,511-191,166,319 , GRCh37.p13 chr2: 192,025,237-192,031,045 STAT4
    nsv6695736copy number variation1nstd229human GRCh38 chr2: 191,124,231-191,128,631 , GRCh37.p13 chr2: 191,988,957-191,993,357 STAT4
    nsv6695315copy number variation1nstd229human GRCh38 chr2: 191,129,201-191,133,900 , GRCh37.p13 chr2: 191,993,927-191,998,626 STAT4
    nsv6693870copy number variation1nstd229human GRCh38 chr2: 191,040,046-191,040,137 , GRCh37.p13 chr2: 191,904,772-191,904,863 STAT4
    nsv6692804copy number variation1nstd229human GRCh38 chr2: 191,129,557-191,470,123 , GRCh37.p13 chr2: 191,994,283-192,334,849 STAT4, LOC105373804, 3 more genes
    nsv6691877copy number variation1nstd229human GRCh38 chr2: 191,124,801-191,126,700 , GRCh37.p13 chr2: 191,989,527-191,991,426 STAT4
    nsv6689645copy number variation1nstd229human GRCh38 chr2: 191,052,671-191,052,696 , GRCh37.p13 chr2: 191,917,397-191,917,422 STAT4
    nsv6688340copy number variation1nstd229human GRCh38 chr2: 191,146,760-191,148,659 , GRCh37.p13 chr2: 192,011,486-192,013,385 STAT4
    nsv6687504copy number variation1nstd229human GRCh38 chr2: 190,894,701-192,994,500 , GRCh37.p13 chr2: 191,759,427-193,859,226 LOC107985785, NABP1, 19 more genes
    nsv6686713copy number variation1nstd229human GRCh38 chr2: 191,154,731-191,154,907 , GRCh37.p13 chr2: 192,019,457-192,019,633 STAT4
    nsv6686637copy number variation1nstd229human GRCh38 chr2: 191,155,356-191,158,156 , GRCh37.p13 chr2: 192,020,082-192,022,882 STAT4
    nsv6686015copy number variation1nstd229human GRCh38 chr2: 191,150,347-191,162,076 , GRCh37.p13 chr2: 192,015,073-192,026,802 STAT4
    nsv6685976copy number variation1nstd229human GRCh38 chr2: 191,170,822-191,173,837 , GRCh37.p13 chr2: 192,035,548-192,038,563 STAT4, HMGB1P27
    nsv6685337copy number variation1nstd229human GRCh38 chr2: 191,130,401-191,133,900 , GRCh37.p13 chr2: 191,995,127-191,998,626 STAT4
    nsv6685151copy number variation1nstd229human GRCh38 chr2: 191,053,001-191,080,500 , GRCh37.p13 chr2: 191,917,727-191,945,226 STAT4
    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