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 149

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5486039copy number variation1nstd206human GRCh38 chr8: 29,203,784-29,219,927 , GRCh37.p13 chr8: 29,061,301-29,077,444 HMGB1P23, KIF13B
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959916copy number variation1nstd200human GRCh38 chr8: 29,216,995-29,217,098 , GRCh37.p13 chr8: 29,074,512-29,074,615 HMGB1P23, KIF13B
    nsv4959915copy number variation1nstd200human GRCh38 chr8: 29,215,885-29,224,489 , GRCh37.p13 chr8: 29,073,402-29,082,006 HMGB1P23, KIF13B
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4157258copy number variation1nstd166human GRCh37.p13 chr8: 29,061,301-29,077,439 , GRCh38.p12 chr8: 29,203,784-29,219,922 HMGB1P23, KIF13B
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 BNIP3L, RNU6-178P, 123 more genes
    nsv3923174copy number variation1nstd102humanPathogenic GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324 RPLP1P9, CHRNA2, 259 more genes
    nsv3922931copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,383,584-36,370,018 , NCBI36 chr8: 12,285,464-36,347,088 , GRCh37 chr8: 12,241,093-36,227,536 LOC105379303, MTND2P32, 361 more genes
    nsv3921773copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,511,855-43,310,472 , GRCh38 chr8: 12,609,975-43,336,172 , GRCh37 chr8: 12,467,484-43,191,315 RPL5P22, ZMAT4, 481 more genes
    nsv3921539copy number variation1nstd102humanPathogenic NCBI36 chr8: 153,682-47,058,107 , GRCh37.p13 chr8: 163,682-46,938,942 , GRCh38.p12 chr8: 213,682-46,027,320 HSPD1P3, RNA5SP253, 770 more genes
    nsv3921035copy number variation2nstd102humanPathogenic GRCh38 chr8: 12,728,904-43,673,207 , GRCh37 chr8: 12,586,413-43,528,350 , NCBI36 chr8: 12,630,784-43,647,507 MIR4287, RNU6-533P, 477 more genes
    nsv3920952copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,452-37,879,246 , GRCh38 chr8: 226,452-38,021,728 , NCBI36 chr8: 166,452-37,998,403 MTUS1, LINC00208, 666 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