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 283

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6850765copy number variation1nstd229human GRCh38 chr8: 38,174,001-38,210,000 , GRCh37.p13 chr8: 38,031,519-38,067,518 LSM1, BAG4
    nsv6846274copy number variation1nstd229human GRCh38 chr8: 38,175,732-38,175,777 , GRCh37.p13 chr8: 38,033,250-38,033,295 BAG4, LSM1
    nsv6842319copy number variation1nstd229human GRCh38 chr8: 38,201,934-38,202,901 , GRCh37.p13 chr8: 38,059,452-38,060,419 BAG4
    nsv6839780copy number variation1nstd229human GRCh38 chr8: 38,193,301-38,198,100 , GRCh37.p13 chr8: 38,050,819-38,055,618 BAG4
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6572754inversion1nstd223human GRCh38 chr8: 38,179,363-38,179,570 , GRCh37.p13 chr8: 38,036,881-38,037,088 BAG4
    nsv6570108inversion1nstd223human GRCh38 chr8: 38,180,374-38,181,090 , GRCh37.p13 chr8: 38,037,892-38,038,608 BAG4
    nsv6569978inversion1nstd223human GRCh38 chr8: 38,190,992-38,191,367 , GRCh37.p13 chr8: 38,048,510-38,048,885 BAG4
    nsv6568537inversion1nstd223human GRCh38 chr8: 38,174,758-38,175,296 , GRCh37.p13 chr8: 38,032,276-38,032,814 BAG4, LSM1
    nsv6566505inversion1nstd223human GRCh38 chr8: 38,184,991-38,185,794 , GRCh37.p13 chr8: 38,042,509-38,043,312 BAG4
    nsv6557175inversion1nstd223human GRCh38 chr8: 38,184,809-38,185,863 , GRCh37.p13 chr8: 38,042,327-38,043,381 BAG4
    nsv6433487copy number variation1nstd223human GRCh38 chr8: 38,193,337-38,198,117 , GRCh37.p13 chr8: 38,050,855-38,055,635 BAG4
    nsv6429010copy number variation1nstd223human GRCh38 chr8: 38,190,015-38,194,996 , GRCh37.p13 chr8: 38,047,533-38,052,514 BAG4
    nsv6428703copy number variation1nstd223human GRCh38 chr8: 38,211,501-38,212,300 , GRCh37.p13 chr8: 38,069,019-38,069,818 BAG4
    nsv6427217copy number variation1nstd223human GRCh38 chr8: 38,198,435-38,308,758 , GRCh37.p13 chr8: 38,055,953-38,166,276 PLPP5, NSD3, 2 more genes
    nsv6425469copy number variation1nstd223human GRCh38 chr8: 38,201,003-38,206,879 , GRCh37.p13 chr8: 38,058,521-38,064,397 BAG4
    nsv6421565copy number variation1nstd223human GRCh38 chr8: 38,196,425-38,198,156 , GRCh37.p13 chr8: 38,053,943-38,055,674 BAG4
    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