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 246

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048217inversion1nstd229human GRCh38 chr5: 65,672,685-65,672,728 , GRCh37.p13 chr5: 64,968,512-64,968,555 SGTB
    nsv7040565inversion1nstd229human GRCh38 chr5: 65,352,482-65,851,740 , GRCh37.p13 chr5: 64,648,309-65,147,568 LOC100419549, RPS2P23, 9 more genes
    nsv6777129copy number variation1nstd229human GRCh38 chr5: 65,517,434-66,063,747 , GRCh37.p13 chr5: 64,813,261-65,359,575 TRIM23, RNU6-540P, 9 more genes
    nsv6776488copy number variation1nstd229human GRCh38 chr5: 65,687,201-65,689,534 , GRCh37.p13 chr5: 64,983,028-64,985,361 SGTB
    nsv6769347copy number variation1nstd229human GRCh38 chr5: 65,677,986-65,683,366 , GRCh37.p13 chr5: 64,973,813-64,979,193 SGTB
    nsv6768826copy number variation1nstd229human GRCh38 chr5: 65,721,232-65,721,631 , GRCh37.p13 chr5: 65,017,059-65,017,458 SGTB, NLN
    nsv6768208copy number variation1nstd229human GRCh38 chr5: 65,703,149-65,708,569 , GRCh37.p13 chr5: 64,998,976-65,004,396 SGTB
    nsv6767987copy number variation1nstd229human GRCh38 chr5: 65,681,663-65,682,009 , GRCh37.p13 chr5: 64,977,490-64,977,836 SGTB
    nsv6765321copy number variation1nstd229human GRCh38 chr5: 65,679,306-65,679,979 , GRCh37.p13 chr5: 64,975,133-64,975,806 SGTB
    nsv6765273copy number variation1nstd229human GRCh38 chr5: 65,460,432-65,973,179 , GRCh37.p13 chr5: 64,756,259-65,269,007 NLN, RNU6-540P, 10 more genes
    nsv6763313copy number variation1nstd229human GRCh38 chr5: 65,613,124-65,679,218 , GRCh37.p13 chr5: 64,908,951-64,975,045 TRAPPC13, SHLD3, 2 more genes
    nsv6758761copy number variation1nstd229human GRCh38 chr5: 65,654,592-65,666,941 , GRCh37.p13 chr5: 64,950,419-64,962,768 SGTB, TRAPPC13
    nsv6573029inversion1nstd223human GRCh38 chr5: 65,667,976-65,668,450 , GRCh37.p13 chr5: 64,963,803-64,964,277 SGTB
    nsv6569104inversion1nstd223human GRCh38 chr5: 65,719,307-65,720,334 , GRCh37.p13 chr5: 65,015,134-65,016,161 SGTB, NLN
    nsv6567691inversion1nstd223human GRCh38 chr5: 65,707,037-65,707,482 , GRCh37.p13 chr5: 65,002,864-65,003,309 SGTB
    nsv6566863inversion1nstd223human GRCh38 chr5: 65,700,982-65,701,685 , GRCh37.p13 chr5: 64,996,809-64,997,512 SGTB
    nsv6564906inversion1nstd223human GRCh38 chr5: 65,708,829-65,709,609 , GRCh37.p13 chr5: 65,004,656-65,005,436 SGTB
    nsv6562891inversion1nstd223human GRCh38 chr5: 65,694,369-65,694,591 , GRCh37.p13 chr5: 64,990,196-64,990,418 SGTB
    nsv6409431copy number variation1nstd223human GRCh38 chr5: 65,677,986-65,683,361 , GRCh37.p13 chr5: 64,973,813-64,979,188 SGTB
    nsv6401638copy number variation1nstd223human GRCh38 chr5: 65,676,840-65,677,804 , GRCh37.p13 chr5: 64,972,667-64,973,631 SGTB
    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