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 757

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146041insertion1nstd232human GRCh37.p13 chr13: 96,633,435-96,633,435 , GRCh38.p12 chr13: 95,981,181-95,981,181 UGGT2
    nsv7137403insertion1nstd232human GRCh37.p13 chr13: 96,633,436-96,633,436 , GRCh38.p12 chr13: 95,981,182-95,981,182 UGGT2
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7066044inversion1nstd229human GRCh38 chr13: 95,529,523-95,830,578 , GRCh37.p13 chr13: 96,181,777-96,482,832 MTND6P18, CLDN10, 8 more genes
    nsv7064814inversion1nstd229human GRCh38 chr13: 96,053,829-96,058,442 , GRCh37.p13 chr13: 96,706,083-96,710,696 UGGT2
    nsv6957835copy number variation1nstd229human GRCh38 chr13: 95,728,901-95,804,200 , GRCh37.p13 chr13: 96,381,155-96,456,454 DNAJC3, UGGT2
    nsv6957806copy number variation1nstd229human GRCh38 chr13: 95,877,301-95,933,100 , GRCh37.p13 chr13: 96,529,555-96,585,354 UGGT2
    nsv6956628copy number variation1nstd229human GRCh38 chr13: 96,038,751-96,734,988 , GRCh37.p13 chr13: 96,691,005-97,387,242 HS6ST3, RN7SL164P, 3 more genes
    nsv6955623copy number variation1nstd229human GRCh38 chr13: 95,838,512-95,845,141 , GRCh37.p13 chr13: 96,490,766-96,497,395 UGGT2
    nsv6955219copy number variation1nstd229human GRCh38 chr13: 95,917,701-95,921,200 , GRCh37.p13 chr13: 96,569,955-96,573,454 UGGT2
    nsv6954938copy number variation1nstd229human GRCh38 chr13: 95,893,001-95,894,800 , GRCh37.p13 chr13: 96,545,255-96,547,054 UGGT2
    nsv6953846copy number variation1nstd229human GRCh38 chr13: 95,937,746-95,941,633 , GRCh37.p13 chr13: 96,590,000-96,593,887 UGGT2
    nsv6953709copy number variation1nstd229human GRCh38 chr13: 95,814,868-95,818,386 , GRCh37.p13 chr13: 96,467,122-96,470,640 UGGT2
    nsv6953583copy number variation1nstd229human GRCh38 chr13: 95,842,049-95,848,299 , GRCh37.p13 chr13: 96,494,303-96,500,553 UGGT2
    nsv6953218copy number variation1nstd229human GRCh38 chr13: 95,930,701-95,934,700 , GRCh37.p13 chr13: 96,582,955-96,586,954 UGGT2
    nsv6953036copy number variation1nstd229human GRCh38 chr13: 95,904,834-95,919,006 , GRCh37.p13 chr13: 96,557,088-96,571,260 UGGT2
    nsv6951827copy number variation1nstd229human GRCh38 chr13: 95,891,844-95,930,680 , GRCh37.p13 chr13: 96,544,098-96,582,934 UGGT2
    nsv6951788copy number variation1nstd229human GRCh38 chr13: 95,890,216-96,156,698 , GRCh37.p13 chr13: 96,542,470-96,808,952 UGGT2, HS6ST3
    nsv6951508copy number variation1nstd229human GRCh38 chr13: 96,053,828-96,060,482 , GRCh37.p13 chr13: 96,706,082-96,712,736 UGGT2
    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