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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916189copy number variation1nstd209human GRCh38 chr8: 121,625,332-121,625,468 , GRCh37.p13 chr8: 122,637,572-122,637,708 HAS2
    nsv5727538mobile element insertion2nstd211human GRCh38 chr8: 121,625,177-121,625,177 , GRCh37.p13 chr8: 122,637,417-122,637,417 HAS2
    nsv5715028mobile element insertion1nstd211human GRCh38 chr8: 121,634,763-121,634,763 , GRCh37.p13 chr8: 122,647,003-122,647,003 HAS2
    nsv5060033copy number variation1nstd102humanUncertain significance GRCh37 chr8: 121,938,227-125,485,728 , GRCh38.p12 chr8: 120,925,987-124,473,487 RNU6-756P, FAM83A, 53 more genes
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4967854copy number variation1nstd200human GRCh38 chr8: 121,621,831-121,623,043 , GRCh37.p13 chr8: 122,634,071-122,635,283 HAS2
    nsv4967853copy number variation1nstd200human GRCh38 chr8: 121,613,186-121,613,301 , GRCh37.p13 chr8: 122,625,426-122,625,541 HAS2
    nsv4965774copy number variation1nstd200human GRCh38 chr8: 121,482,414-122,511,336 , GRCh37.p13 chr8: 122,494,654-123,523,575 LINC02855, HAS2, 5 more genes
    nsv4965772copy number variation1nstd200human GRCh38 chr8: 121,462,767-121,613,554 , GRCh37.p13 chr8: 122,475,007-122,625,794 HAS2
    nsv4827929copy number variation1nstd200human GRCh37 chr8: 122,637,572-122,637,709 , GRCh38.p12 chr8: 121,625,332-121,625,469 HAS2
    nsv4827928copy number variation1nstd200human GRCh37 chr8: 122,634,071-122,635,283 , GRCh38.p12 chr8: 121,621,831-121,623,043 HAS2
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 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
    nsv4675222copy number variation1nstd102humanPathogenic GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134 LOC105375723, CSMD3, 93 more genes
    nsv4572943mobile element insertion1nstd166human GRCh37.p13 chr8: 122,637,400-122,637,400 , GRCh38.p12 chr8: 121,625,160-121,625,160 HAS2
    nsv4545545insertion1nstd166human GRCh37.p13 chr8: 122,645,111-122,645,111 , GRCh38.p12 chr8: 121,632,871-121,632,871 HAS2
    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
    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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