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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5247240copy number variation1nstd204human GRCh38.p13 chr8: 143,641,501-143,860,200 , GRCh37.p13 chr8|NW_003315923.1: 1-198,845 , GRCh37.p13 chr8: 144,744,709-144,940,217 LOC105375799, FAM83H, 16 more genes
    nsv5241991copy number variation1nstd204human GRCh37.p13 chr8|NW_003315923.1: 89,346-217,145 , GRCh37.p13 chr8: 144,832,871-144,952,668 , GRCh38.p13 chr8: 143,750,701-143,878,500 PUF60, SCRIB, 7 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
    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
    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
    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
    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
    nsv4455260copy number variation1nstd102humanUncertain significance GRCh37 chr8: 144,190,206-146,295,771 , GRCh38.p12 chr8: 143,108,789-145,070,385 COMMD5, RHPN1-AS1, 113 more genes
    nsv4349929copy number variation1nstd102humanPathogenic GRCh37 chr8: 144,879,444-145,199,846 , GRCh38.p12 chr8: 143,797,274-144,144,943 TSSK5P, HGH1, 22 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
    nsv3964483insertion1nstd168human GRCh38 chr8: 143,814,170-143,918,472 , GRCh37.p13 chr8: 144,910,965-144,992,640 , GRCh37.p13 chr8|NW_003315923.1: 152,815-257,117 PLEC, PUF60, 5 more genes
    nsv3962546copy number variation1nstd168human GRCh38 chr8: 143,814,170-143,872,354 , GRCh37.p13 chr8|NW_003315923.1: 152,815-210,999 , GRCh37.p13 chr8: 144,910,965-144,946,522 PUF60, SCRIB, 4 more genes
    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
    nsv3924581copy number variation1nstd102humanPathogenic NCBI36 chr8: 144,838,977-145,482,487 , GRCh37 chr8: 144,940,777-145,511,679 , GRCh38 chr8: 143,684,819-144,287,978 SCX, MIR6847, 35 more genes
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