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 180

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5627242insertion1nstd207human GRCh38 chr8: 142,639,398-142,639,398 , GRCh37.p13 chr8|NW_003871066.2: 9,531-9,531 , GRCh37.p13 chr8: 143,720,751-143,720,751 LOC101928087
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 more genes
    nsv4675692copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,570,920-144,459,613 , GRCh38.p12 chr8: 142,489,559-143,377,443 SLURP2, THEM6, 37 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 more genes
    nsv4674996copy number variation1nstd102humanPathogenic GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610 POU5F1B, DNAJC8P3, 158 more genes
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4456083copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,988,974-144,218,537 , GRCh38.p12 chr8: 141,907,613-143,137,120 LY6E, CYP11B2, 32 more genes
    nsv4455524copy number variation1nstd102humanPathogenic GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385 LINC00051, LOC107986982, 197 more genes
    nsv4399968copy number variation1nstd174human GRCh37 chr8: 143,136,801-144,016,864 , GRCh38.p12 chr8: 142,055,440-142,935,448 , RN7SL260P, 24 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
    nsv4331387inversion1nstd166human GRCh37.p13 chr8: 142,092,526-144,206,149 , GRCh38.p12 chr8: 141,082,427-143,124,732 , ADGRB1, 49 more genes
    nsv4165959copy number variation1nstd166human GRCh37.p13 chr8: 143,720,767-143,720,821 , GRCh38.p12 chr8: 142,639,414-142,639,444 LOC101928087
    nsv4159740copy number variation1nstd166human GRCh37.p13 chr8: 143,714,909-143,720,932 , GRCh38.p12 chr8: 142,633,558-142,639,555 LOC101928087
    nsv3967111copy number variation1nstd168human GRCh38 chr8: 142,635,506-142,662,218 , GRCh37.p13 chr8|NW_003871066.2: 5,639-32,351 , GRCh37.p13 chr8: 143,716,857-143,743,630 LOC101928087, JRK
    nsv3924756copy number variation1nstd102humanPathogenic NCBI36 chr8: 143,280,736-145,148,886 , GRCh38 chr8: 142,201,468-144,002,730 , GRCh37 chr8: 143,282,829-145,076,898 MROH4P, LINC00051, 77 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