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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5722628mobile element insertion2nstd211human GRCh38 chr9: 70,162,494-70,162,494 , GRCh37.p13 chr9: 72,777,410-72,777,410 MAMDC2, MAMDC2-AS1
    nsv5628491insertion1nstd207human GRCh38 chr9: 70,162,494-70,162,494 , GRCh37.p13 chr9: 72,777,410-72,777,410 MAMDC2-AS1, MAMDC2
    nsv5559907mobile element insertion1nstd206human GRCh38 chr9: 70,162,506-70,162,524 , GRCh37.p13 chr9: 72,777,422-72,777,440 MAMDC2, MAMDC2-AS1
    nsv5540022insertion1nstd206human GRCh38 chr9: 70,157,195-70,157,246 , GRCh37.p13 chr9: 72,772,111-72,772,162 MAMDC2-AS1, MAMDC2
    nsv5485355copy number variation1nstd206human GRCh38 chr9: 70,159,270-70,159,550 , GRCh37.p13 chr9: 72,774,186-72,774,466 MAMDC2, MAMDC2-AS1
    nsv5199189mobile element insertion1nstd203human GRCh38 chr9: 70,162,496-70,162,506 , GRCh37.p13 chr9: 72,777,412-72,777,422 MAMDC2-AS1, MAMDC2
    nsv5197933mobile element insertion1nstd203human GRCh38 chr9: 70,162,499-70,162,506 , GRCh37.p13 chr9: 72,777,415-72,777,422 MAMDC2-AS1, MAMDC2
    nsv5191281mobile element insertion1nstd203human GRCh38 chr9: 70,162,501-70,162,506 , GRCh37.p13 chr9: 72,777,417-72,777,422 MAMDC2, MAMDC2-AS1
    nsv5189631mobile element insertion1nstd203human GRCh38 chr9: 70,162,494-70,162,506 , GRCh37.p13 chr9: 72,777,410-72,777,422 MAMDC2, MAMDC2-AS1
    nsv5187274mobile element insertion1nstd203human GRCh38 chr9: 70,162,497-70,162,506 , GRCh37.p13 chr9: 72,777,413-72,777,422 MAMDC2, MAMDC2-AS1
    nsv5186647mobile element insertion1nstd203human GRCh38 chr9: 70,162,495-70,162,506 , GRCh37.p13 chr9: 72,777,411-72,777,422 MAMDC2-AS1, MAMDC2
    nsv5185346mobile element insertion1nstd203human GRCh38 chr9: 70,162,498-70,162,506 , GRCh37.p13 chr9: 72,777,414-72,777,422 MAMDC2, MAMDC2-AS1
    nsv5184661mobile element insertion1nstd203human GRCh38 chr9: 70,163,214-70,163,229 , GRCh37.p13 chr9: 72,778,130-72,778,145 MAMDC2, MAMDC2-AS1
    nsv5183160mobile element insertion1nstd203human GRCh38 chr9: 70,162,489-70,162,506 , GRCh37.p13 chr9: 72,777,405-72,777,422 MAMDC2, MAMDC2-AS1
    nsv5180641mobile element insertion1nstd203human GRCh38 chr9: 70,162,500-70,162,506 , GRCh37.p13 chr9: 72,777,416-72,777,422 MAMDC2, MAMDC2-AS1
    nsv4760543insertion1nstd199human GRCh37 chr9: 72,777,420-72,777,420 , GRCh38.p12 chr9: 70,162,504-70,162,504 , GRCh38.p12 chr9|NW_003315930.1: 138,375-138,375 MAMDC2, MAMDC2-AS1
    nsv4695713mobile element insertion1nstd186human GRCh37 chr9: 72,777,422-72,777,422 , GRCh38.p12 chr9: 70,162,506-70,162,506 , GRCh38.p12 chr9|NW_003315930.1: 138,377-138,377 MAMDC2-AS1, MAMDC2
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456140copy number variation1nstd102humanUncertain significance GRCh37 chr9: 72,519,550-73,191,986 , GRCh38.p12 chr9: 69,904,634-70,577,070 TRPM3, RPL24P8, 9 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
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