Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145714insertion1nstd232human GRCh37.p13 chr6: 109,690,223-109,690,223 , GRCh38.p12 chr6: 109,369,020-109,369,020 CD164
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv7097033copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,690,054-110,266,416 , GRCh38.p12 chr6: 109,368,851-109,945,213 MICAL1, ZBTB24, 6 more genes
    nsv7055005inversion1nstd229human GRCh38 chr6: 108,167,886-110,172,775 , GRCh37.p13 chr6: 108,489,090-110,493,978 AK9, WASF1, 34 more genes
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6809456copy number variation1nstd229human GRCh38 chr6: 109,380,401-109,512,000 , GRCh37.p13 chr6: 109,701,604-109,833,203 PPIL6, AK9, 5 more genes
    nsv6808442copy number variation1nstd229human GRCh38 chr6: 109,333,960-109,365,077 , GRCh37.p13 chr6: 109,655,163-109,686,280 CCDC162P, CD164
    nsv6808155copy number variation1nstd229human GRCh38 chr6: 109,373,166-109,380,505 , GRCh37.p13 chr6: 109,694,369-109,701,708 CD164
    nsv6805716copy number variation1nstd229human GRCh38 chr6: 109,328,901-109,364,800 , GRCh37.p13 chr6: 109,650,104-109,686,003 CCDC162P, CD164
    nsv6805143copy number variation1nstd229human GRCh38 chr6: 109,373,855-109,375,957 , GRCh37.p13 chr6: 109,695,058-109,697,160 CD164
    nsv6802736copy number variation1nstd229human GRCh38 chr6: 109,364,008-109,365,548 , GRCh37.p13 chr6: 109,685,211-109,686,751 CD164
    nsv6799509copy number variation1nstd229human GRCh38 chr6: 109,282,211-109,485,074 , GRCh37.p13 chr6: 109,603,414-109,806,277 ZBTB24-DT, SMPD2, 8 more genes
    nsv6798389copy number variation1nstd229human GRCh38 chr6: 109,382,001-109,511,500 , GRCh37.p13 chr6: 109,703,204-109,832,703 PPIL6, AK9, 5 more genes
    nsv6637155copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,576,603-109,878,834 , GRCh38.p12 chr6: 109,255,400-109,557,631 RNY3P11, ZBTB24, 9 more genes
    nsv6613236copy number variation1nstd223human GRCh38 chr6: 109,381,301-109,383,400 , GRCh37.p13 chr6: 109,702,504-109,704,603 CD164
    nsv6611847copy number variation1nstd223human GRCh38 chr6: 109,381,901-109,382,900 , GRCh37.p13 chr6: 109,703,104-109,704,103 CD164
    nsv6609606copy number variation1nstd223human GRCh38 chr6: 109,367,301-109,368,300 , GRCh37.p13 chr6: 109,688,504-109,689,503 CD164
    nsv6606041copy number variation1nstd223human GRCh38 chr6: 109,333,960-109,365,073 , GRCh37.p13 chr6: 109,655,163-109,686,276 CCDC162P, CD164
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    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