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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925116copy number variation1nstd209human GRCh38 chr8: 144,849,773-144,849,857 , GRCh37.p13 chr8: 146,075,158-146,075,242 COMMD5
    nsv5721002mobile element insertion1nstd211human GRCh38 chr8: 144,846,880-144,846,880 , GRCh37.p13 chr8: 146,072,265-146,072,265 COMMD5, ZNF7
    nsv5642033insertion2nstd207human GRCh38 chr8: 144,838,976-144,838,976 , GRCh37.p13 chr8: 146,064,361-146,064,361 COMMD5, ZNF7
    nsv5596098copy number variation1nstd207human GRCh38 chr8: 144,838,976-144,839,045 , GRCh37.p13 chr8: 146,064,361-146,064,430 COMMD5, ZNF7
    nsv5481053copy number variation1nstd206human GRCh38 chr8: 144,843,353-144,844,436 , GRCh37.p13 chr8: 146,068,738-146,069,821 COMMD5, ZNF7
    nsv5475341copy number variation1nstd206human GRCh38 chr8: 144,849,774-144,849,858 , GRCh37.p13 chr8: 146,075,159-146,075,243 COMMD5
    nsv5100445mobile element insertion1nstd203human GRCh38 chr8: 144,853,657-144,853,667 , GRCh37.p13 chr8: 146,079,042-146,079,052 COMMD5
    nsv4969186copy number variation1nstd200human GRCh38 chr8: 144,827,882-144,873,461 , GRCh37.p13 chr8: 146,053,267-146,098,846 ZNF7, COMMD5
    nsv4962757copy number variation1nstd200human GRCh38 chr8: 144,843,327-144,844,628 , GRCh37.p13 chr8: 146,068,712-146,070,013 ZNF7, COMMD5
    nsv4962747copy number variation1nstd200human GRCh38 chr8: 144,806,568-144,839,967 , GRCh37.p13 chr8: 146,031,953-146,065,352 ZNF7, ZNF517, 2 more genes
    nsv4813939copy number variation1nstd200human GRCh37 chr8: 146,068,737-146,069,822 , GRCh38.p12 chr8: 144,843,352-144,844,437 COMMD5, ZNF7
    nsv4813932copy number variation1nstd200human GRCh37 chr8: 146,031,953-146,065,352 , GRCh38.p12 chr8: 144,806,568-144,839,967 COMMD5, LOC100130027, 2 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
    nsv4759293insertion1nstd199human GRCh37 chr8: 146,064,393-146,064,393 , GRCh38.p12 chr8: 144,839,008-144,839,008 ZNF7, COMMD5
    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
    nsv4641438copy number variation1nstd186human GRCh37 chr8: 146,075,159-146,075,243 , GRCh38.p12 chr8: 144,849,774-144,849,858 COMMD5
    nsv4608884copy number variation1nstd183human GRCh37 chr8: 146,070,554-146,298,155 , GRCh38.p12 chr8: 144,845,169-145,072,769 ZNF7, ZNF16, 7 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
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