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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5635775insertion1nstd207human GRCh38 chr8: 144,262,769-144,262,769 , GRCh37.p13 chr8|NW_003315924.1: 32,028-32,028 MIR7112, BOP1
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
    nsv5248548copy number variation1nstd204human GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784 MIR661, EXOSC4, 51 more genes
    nsv4969167copy number variation1nstd200human GRCh38 chr8: 144,234,119-144,267,165 , GRCh37.p13 chr8|NW_003315924.1: 3,378-36,424 MIR7112, BOP1, 2 more genes
    nsv4962695copy number variation1nstd200human GRCh38 chr8: 144,258,799-144,261,357 , GRCh37.p13 chr8|NW_003315924.1: 28,058-30,616 BOP1, MROH1, 1 more genes
    nsv4769373copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551 ZFTRAF1, PLEC, 68 more genes
    nsv4745440copy number variation1nstd199human GRCh38.p12 chr8: 144,133,005-144,269,397 , GRCh37 chr8: 145,187,908-145,433,122 BOP1, HGH1, 4 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
    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
    nsv4675215copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,287,199-145,705,521 , GRCh38.p12 chr8: 144,232,296-144,480,138 BOP1, FOXH1, 25 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
    nsv4673054copy number variation2nstd186human GRCh37 chr8: 145,303,399-145,499,070 , GRCh38.p12 chr8: 144,132,479-144,277,712 BOP1, HGH1, 4 more genes
    nsv4650869copy number variation1nstd186human GRCh37 chr8: 145,480,000-145,502,750 , GRCh38.p12 chr8: 144,256,044-144,269,397 BOP1, SCX, 2 more genes
    nsv4648664copy number variation1nstd186human GRCh37 chr8: 145,312,850-145,332,400 , GRCh38.p12 chr8: 144,257,947-144,269,397 BOP1, SCX, 2 more genes
    nsv4600902copy number variation2nstd183human GRCh37 chr8: 145,303,399-145,499,070 , GRCh38.p12 chr8: 144,132,479-144,277,712 BOP1, HGH1, 4 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
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