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 401

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147561copy number variation1nstd232human GRCh37.p13 chr1: 227,163,840-227,163,919 , GRCh38.p12 chr1: 226,976,139-226,976,218 COQ8A
    nsv7139316copy number variation1nstd232human GRCh37.p13 chr1: 227,165,903-227,165,978 , GRCh38.p12 chr1: 226,978,202-226,978,277 COQ8A
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7052421inversion1nstd229human GRCh38 chr1: 226,974,131-226,974,217 , GRCh37.p13 chr1: 227,161,832-227,161,918 COQ8A
    nsv7049731inversion1nstd229human GRCh38 chr1: 226,948,922-226,949,023 , GRCh37.p13 chr1: 227,136,623-227,136,724 COQ8A
    nsv6677685copy number variation1nstd229human GRCh38 chr1: 226,979,630-226,980,390 , GRCh37.p13 chr1: 227,167,331-227,168,091 COQ8A
    nsv6676122copy number variation1nstd229human GRCh38 chr1: 226,968,901-226,974,200 , GRCh37.p13 chr1: 227,156,602-227,161,901 COQ8A
    nsv6676025copy number variation1nstd229human GRCh38 chr1: 226,984,641-226,989,202 , GRCh37.p13 chr1: 227,172,342-227,176,903 COQ8A, CDC42BPA
    nsv6675777copy number variation1nstd229human GRCh38 chr1: 226,939,201-226,940,300 , GRCh37.p13 chr1: 227,126,902-227,128,001 COQ8A
    nsv6675202copy number variation1nstd229human GRCh38 chr1: 226,961,768-226,969,034 , GRCh37.p13 chr1: 227,149,469-227,156,735 COQ8A
    nsv6673604copy number variation1nstd229human GRCh38 chr1: 226,969,522-226,971,389 , GRCh37.p13 chr1: 227,157,223-227,159,090 COQ8A
    nsv6672070copy number variation1nstd229human GRCh38 chr1: 226,978,202-226,978,278 , GRCh37.p13 chr1: 227,165,903-227,165,979 COQ8A
    nsv6670112copy number variation1nstd229human GRCh38 chr1: 226,947,926-226,957,499 , GRCh37.p13 chr1: 227,135,627-227,145,200 COQ8A
    nsv6669587copy number variation1nstd229human GRCh38 chr1: 226,953,611-226,961,071 , GRCh37.p13 chr1: 227,141,312-227,148,772 COQ8A
    nsv6664301copy number variation1nstd229human GRCh38 chr1: 226,937,217-226,944,684 , GRCh37.p13 chr1: 227,124,918-227,132,385 COQ8A
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6544022inversion1nstd223human GRCh38 chr1: 226,971,112-226,971,523 , GRCh37.p13 chr1: 227,158,813-227,159,224 COQ8A
    nsv6335130copy number variation1nstd223human GRCh38 chr1: 226,937,217-226,944,724 , GRCh37.p13 chr1: 227,124,918-227,132,425 COQ8A
    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