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 394

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv6937047copy number variation1nstd229human GRCh38 chr13: 26,196,101-26,199,300 , GRCh37.p13 chr13: 26,770,238-26,773,437 RNF6
    nsv6936537copy number variation1nstd229human GRCh38 chr13: 26,193,475-26,193,533 , GRCh37.p13 chr13: 26,767,612-26,767,670 RNF6
    nsv6933078copy number variation1nstd229human GRCh38 chr13: 26,196,318-26,199,246 , GRCh37.p13 chr13: 26,770,455-26,773,383 RNF6
    nsv6932195copy number variation1nstd229human GRCh38 chr13: 26,196,514-26,199,250 , GRCh37.p13 chr13: 26,770,651-26,773,387 RNF6
    nsv6932076copy number variation1nstd229human GRCh38 chr13: 26,014,684-26,150,533 , GRCh37.p13 chr13: 26,588,822-26,724,671 ATP8A2, PRUNE1P1, 4 more genes
    nsv6930849copy number variation1nstd229human GRCh38 chr13: 26,197,498-26,199,112 , GRCh37.p13 chr13: 26,771,635-26,773,249 RNF6
    nsv6928845copy number variation1nstd229human GRCh38 chr13: 26,169,576-26,177,397 , GRCh37.p13 chr13: 26,743,713-26,751,534 RNF6
    nsv6928658copy number variation1nstd229human GRCh38 chr13: 26,009,101-26,217,600 , GRCh37.p13 chr13: 26,583,239-26,791,737 SHISA2, LINC00415, 4 more genes
    nsv6927708copy number variation1nstd229human GRCh38 chr13: 26,184,757-26,327,926 , GRCh37.p13 chr13: 26,758,894-26,902,063 CDK8, THAP12P6, 1 more genes
    nsv6927467copy number variation1nstd229human GRCh38 chr13: 26,146,101-26,154,700 , GRCh37.p13 chr13: 26,720,239-26,728,838 RNF6, ATP8A2P3
    nsv6925732copy number variation1nstd229human GRCh38 chr13: 26,187,134-26,187,172 , GRCh37.p13 chr13: 26,761,271-26,761,309 RNF6
    nsv6922778copy number variation1nstd229human GRCh38 chr13: 26,176,666-26,185,512 , GRCh37.p13 chr13: 26,750,803-26,759,649 RNF6
    nsv6922278copy number variation1nstd229human GRCh38 chr13: 26,083,143-26,161,925 , GRCh37.p13 chr13: 26,657,281-26,736,062 RNF6, PRUNE1P1, 1 more genes
    nsv6922245copy number variation1nstd229human GRCh38 chr13: 26,210,651-26,214,684 , GRCh37.p13 chr13: 26,784,788-26,788,821 RNF6
    nsv6922024copy number variation1nstd229human GRCh38 chr13: 26,222,859-26,228,581 , GRCh37.p13 chr13: 26,796,996-26,802,718 RNF6
    nsv6921625copy number variation1nstd229human GRCh38 chr13: 26,163,728-26,169,897 , GRCh37.p13 chr13: 26,737,865-26,744,034 RNF6
    nsv6921173copy number variation1nstd229human GRCh38 chr13: 26,144,778-26,144,971 , GRCh37.p13 chr13: 26,718,916-26,719,109 ATP8A2P3, RNF6
    nsv6921124copy number variation1nstd229human GRCh38 chr13: 26,220,105-26,233,202 , GRCh37.p13 chr13: 26,794,242-26,807,339 RNF6, THAP12P6
    nsv6920502copy number variation1nstd229human GRCh38 chr13: 26,197,501-26,199,000 , GRCh37.p13 chr13: 26,771,638-26,773,137 RNF6
    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