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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5638803insertion1nstd207human GRCh38 chr8: 143,721,124-143,721,124 , GRCh37.p13 chr8|NW_003315923.1: 59,769-59,769 , GRCh37.p13 chr8: 144,803,294-144,803,294 MAPK15
    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
    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
    nsv4813895copy number variation1nstd200human GRCh37 chr8: 144,800,836-144,802,355 , GRCh38.p12 chr8: 143,718,666-143,720,185 , GRCh38.p12 chr8|NT_187571.1: 195,713-197,232 MAPK15
    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
    nsv4674965copy number variation1nstd102humanLikely benign GRCh37 chr8: 144,754,114-144,857,373 , GRCh38.p12 chr8: 143,671,944-143,775,203 , GRCh38.p12 chr8|NT_187571.1: 148,991-252,250 MAPK15, ZNF707, 7 more genes
    nsv4612543copy number variation1nstd183human GRCh37 chr8: 144,803,761-144,803,856 , GRCh38.p12 chr8|NT_187571.1: 198,638-198,733 , GRCh38.p12 chr8: 143,721,591-143,721,686 MAPK15
    nsv4602236copy number variation1nstd183human GRCh37 chr8: 144,772,844-144,823,911 , GRCh38.p12 chr8: 143,690,674-143,741,741 , GRCh38.p12 chr8|NT_187571.1: 167,721-218,788 MAPK15, ZNF707, 5 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
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
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