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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5486305copy number variation1nstd206human GRCh38 chr8: 143,335,028-143,429,075 , GRCh37.p13 chr8: 144,417,198-144,511,245 RHPN1-AS1, RHPN1, 5 more genes
    nsv5310506copy number variation1nstd204human GRCh37.p13 chr8: 144,413,633-144,475,007 , GRCh38.p13 chr8: 143,331,463-143,392,837 RHPN1-AS1, RHPN1, 2 more genes
    nsv5301183copy number variation1nstd204human GRCh38.p13 chr8: 143,160,494-143,803,360 , GRCh37.p13 chr8: 144,241,911-144,743,529 TIGD5, MAPK15, 36 more genes
    nsv5254948copy number variation1nstd204human GRCh38.p13 chr8: 143,167,001-143,860,200 , GRCh37.p13 chr8: 144,248,418-144,743,525 LOC105375798, LINC02990, 41 more genes
    nsv5253030copy number variation1nstd204human GRCh38.p13 chr8: 143,160,501-143,441,400 , GRCh37.p13 chr8: 144,241,918-144,523,570 MAFA-AS1, TOP1MT, 13 more genes
    nsv5246965copy number variation1nstd204human GRCh38.p13 chr8: 143,330,656-143,371,857 , GRCh37.p13 chr8: 144,412,826-144,454,027 RNU6-220P, RHPN1, 2 more genes
    nsv5246709copy number variation1nstd204human GRCh38.p13 chr8: 143,331,501-143,391,900 , GRCh37.p13 chr8: 144,413,671-144,474,070 TOP1MT, RNU6-220P, 2 more genes
    nsv4962632copy number variation1nstd200human GRCh38 chr8: 143,358,718-143,389,691 , GRCh37.p13 chr8: 144,440,888-144,471,861 RHPN1, RHPN1-AS1, 1 more genes
    nsv4813880copy number variation1nstd200human GRCh37 chr8: 144,413,637-144,475,004 , GRCh38.p12 chr8: 143,331,467-143,392,834 RNU6-220P, RHPN1, 2 more genes
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4729040copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,285,728-144,534,781 , GRCh38.p12 chr8: 143,204,267-143,452,611 GPIHBP1, ZNF696, 11 more genes
    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
    nsv4674833copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,320,365-144,624,272 , GRCh38.p12 chr8: 143,238,195-143,542,102 ZFP41, RHPN1-AS1, 12 more genes
    nsv4526405copy number variation1nstd166human GRCh37.p13 chr8: 144,443,000-144,449,000 , GRCh38.p12 chr8: 143,360,830-143,366,830 RHPN1, RHPN1-AS1
    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
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