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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
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5508630copy number variation1nstd206human GRCh38 chr10: 123,055,206-123,056,229 , GRCh37.p13 chr10: 124,814,722-124,815,745 ACADSB
    nsv5503320copy number variation1nstd206human GRCh38 chr10: 123,012,642-123,012,701 , GRCh37.p13 chr10: 124,772,158-124,772,217 ACADSB
    nsv5309275copy number variation1nstd204human GRCh38.p13 chr10: 123,055,246-123,056,238 , GRCh37.p13 chr10: 124,814,762-124,815,754 ACADSB
    nsv5139140mobile element insertion1nstd203human GRCh38 chr10: 123,045,171-123,045,196 , GRCh37.p13 chr10: 124,804,687-124,804,712 ACADSB
    nsv5130367mobile element insertion1nstd203human GRCh38 chr10: 123,045,158-123,045,171 , GRCh37.p13 chr10: 124,804,674-124,804,687 ACADSB
    nsv5125615mobile element insertion1nstd203human GRCh38 chr10: 123,045,144-123,045,159 , GRCh37.p13 chr10: 124,804,660-124,804,675 ACADSB
    nsv4977326copy number variation1nstd200human GRCh38 chr10: 123,032,881-123,034,039 , GRCh37.p13 chr10: 124,792,397-124,793,555 ACADSB
    nsv4974106copy number variation1nstd200human GRCh38 chr10: 123,040,940-123,233,195 , GRCh37.p13 chr10: 124,800,456-124,992,711 HMX2, HMX3, 4 more genes
    nsv4849290copy number variation1nstd200human GRCh37 chr10: 124,814,777-124,815,755 , GRCh38.p12 chr10: 123,055,261-123,056,239 ACADSB
    nsv4836080copy number variation1nstd200human GRCh37 chr10: 124,792,397-124,793,555 , GRCh38.p12 chr10: 123,032,881-123,034,039 ACADSB
    nsv4679699copy number variation1nstd189human GRCh37.p13 chr10: 124,478,359-125,318,025 , GRCh38.p12 chr10: 122,718,843-123,558,509 ACADSB, HMX2, 15 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4670983copy number variation1nstd186human GRCh37 chr10: 124,814,697-124,815,745 , GRCh38.p12 chr10: 123,055,181-123,056,229 ACADSB
    nsv4605572copy number variation1nstd183human GRCh37 chr10: 124,812,829-124,816,420 , GRCh38.p12 chr10: 123,053,313-123,056,904 ACADSB
    nsv4600922copy number variation1nstd183human GRCh37 chr10: 124,797,235-124,799,934 , GRCh38.p12 chr10: 123,037,719-123,040,418 ACADSB
    nsv4600033copy number variation1nstd183human GRCh37 chr10: 124,814,697-124,815,745 , GRCh38.p12 chr10: 123,055,181-123,056,229 ACADSB
    nsv4551069insertion1nstd166human GRCh37.p13 chr10: 124,804,647-124,804,647 , GRCh38.p12 chr10: 123,045,131-123,045,131 ACADSB
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