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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711902mobile element insertion1nstd211human GRCh38 chr8: 121,667,989-121,667,989 , GRCh37.p13 chr8: 122,680,229-122,680,229 LINC02855
    nsv5484332copy number variation1nstd206human GRCh38 chr8: 121,679,446-121,682,873 , GRCh37.p13 chr8: 122,691,686-122,695,113 LINC02855
    nsv5483225copy number variation1nstd206human GRCh38 chr8: 121,667,130-121,667,283 , GRCh37.p13 chr8: 122,679,370-122,679,523 LINC02855
    nsv5401862mobile element insertion1nstd206human GRCh38 chr8: 121,667,972-121,667,977 , GRCh37.p13 chr8: 122,680,212-122,680,217 LINC02855
    nsv5318093copy number variation1nstd204human GRCh38.p13 chr8: 121,669,090-121,911,876 , GRCh37.p13 chr8: 122,681,330-122,924,115 LINC02855
    nsv5257406copy number variation1nstd204human GRCh38.p13 chr8: 121,669,351-121,696,848 , GRCh37.p13 chr8: 122,681,591-122,709,088 LINC02855
    nsv5251593copy number variation1nstd204human GRCh38.p13 chr8: 121,671,151-121,672,350 , GRCh37.p13 chr8: 122,683,391-122,684,590 LINC02855
    nsv5248161copy number variation1nstd204human GRCh38.p13 chr8: 121,670,851-121,671,950 , GRCh37.p13 chr8: 122,683,091-122,684,190 LINC02855
    nsv5246061copy number variation1nstd204human GRCh38.p13 chr8: 121,669,101-121,911,000 , GRCh37.p13 chr8: 122,681,341-122,923,239 LINC02855
    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
    nsv4967856copy number variation1nstd200human GRCh38 chr8: 121,685,048-121,686,062 , GRCh37.p13 chr8: 122,697,288-122,698,302 LINC02855
    nsv4967855copy number variation1nstd200human GRCh38 chr8: 121,669,117-121,911,852 , GRCh37.p13 chr8: 122,681,357-122,924,091 LINC02855
    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
    nsv4827931copy number variation1nstd200human GRCh37 chr8: 122,697,288-122,698,302 , GRCh38.p12 chr8: 121,685,048-121,686,062 LINC02855
    nsv4827930copy number variation1nstd200human GRCh37 chr8: 122,681,358-122,924,092 , GRCh38.p12 chr8: 121,669,118-121,911,853 LINC02855
    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
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