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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5707640mobile element insertion1nstd211human GRCh38 chr8: 142,739,043-142,739,043 , GRCh37.p13 chr8: 143,820,461-143,820,461 SLURP1
    nsv5395257mobile element insertion1nstd206human GRCh38 chr8: 142,739,043-142,739,094 , GRCh37.p13 chr8: 143,820,461-143,820,512 SLURP1
    nsv4813852copy number variation1nstd200human GRCh37 chr8: 143,821,837-143,821,919 , GRCh38.p12 chr8: 142,740,419-142,740,501 SLURP1
    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
    nsv4674889copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,728,492-144,093,928 , GRCh38.p12 chr8: 142,647,108-143,012,511 THEM6, LNCOC1, 16 more genes
    nsv4612155copy number variation1nstd183human GRCh37 chr8: 143,798,552-143,933,170 , GRCh38.p12 chr8: 142,717,134-142,851,754 GML, LY6D, 7 more genes
    nsv4485086mobile element insertion1nstd166human GRCh37.p13 chr8: 143,820,450-143,820,450 , GRCh38.p12 chr8: 142,739,032-142,739,032 SLURP1
    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
    nsv4456284copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,786,100-143,964,656 , GRCh38.p12 chr8: 142,704,682-142,883,240 CYP11B1, LY6D, 10 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
    nsv4401104copy number variation1nstd174human GRCh37 chr8: 143,798,552-143,933,158 , GRCh38.p12 chr8: 142,717,134-142,851,742 GML, LY6D, 7 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
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