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 210

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7073126inversion1nstd229human GRCh38 chr8: 27,092,704-27,554,548 , GRCh37.p13 chr8: 26,950,221-27,412,065 STMN4, LOC105379340, 5 more genes
    nsv7065905inversion1nstd229human GRCh38 chr8: 27,302,453-27,302,481 , GRCh37.p13 chr8: 27,159,970-27,159,998 TRIM35
    nsv6856527copy number variation1nstd229human GRCh38 chr8: 27,298,444-27,309,080 , GRCh37.p13 chr8: 27,155,961-27,166,597 TRIM35
    nsv6854430copy number variation1nstd229human GRCh38 chr8: 27,295,838-27,309,657 , GRCh37.p13 chr8: 27,153,355-27,167,174 PTK2B, TRIM35
    nsv6851316copy number variation1nstd229human GRCh38 chr8: 27,274,789-27,283,572 , GRCh37.p13 chr8: 27,132,306-27,141,089 TRIM35
    nsv6845218copy number variation1nstd229human GRCh38 chr8: 27,311,701-27,315,265 , GRCh37.p13 chr8: 27,169,218-27,172,782 PTK2B, TRIM35
    nsv6844824copy number variation1nstd229human GRCh38 chr8: 27,305,431-27,370,660 , GRCh37.p13 chr8: 27,162,948-27,228,177 PTK2B, TRIM35
    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
    nsv6636640copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,064,033-28,832,392 , GRCh38.p12 chr8: 27,206,516-28,974,875 ZNF395, PNOC, 39 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6430189copy number variation1nstd223human GRCh38 chr8: 27,256,321-27,295,808 , GRCh37.p13 chr8: 27,113,838-27,153,325 TRIM35, STMN4
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6137272copy number variation1nstd213human GRCh37 chr8: 26,370,000-35,590,001 , GRCh38.p12 chr8: 26,512,484-35,732,483 ADRA1A, CHRNA2, 141 more genes
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
    nsv6136662copy number variation1nstd213human GRCh37 chr8: 27,060,000-27,170,001 , GRCh38.p12 chr8: 27,202,483-27,312,484 PTK2B, TRIM35, 2 more genes
    nsv6136655copy number variation1nstd213human GRCh37 chr8: 19,630,000-29,910,001 , GRCh38.p12 chr8: 19,772,489-30,052,485 BMP1, BNIP3L, 194 more genes
    nsv6136573copy number variation1nstd213human GRCh37 chr8: 25,790,000-30,640,001 , GRCh38.p12 chr8: 25,932,484-30,782,485 EPHX2, GSR, 99 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