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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5893828copy number variation1nstd209human GRCh38 chr5: 43,479,000-43,482,325 , GRCh37.p13 chr5: 43,479,102-43,482,427 C5orf34-AS1, TMEM267
    nsv5889110copy number variation1nstd209human GRCh38 chr5: 43,484,166-43,486,919 , GRCh37.p13 chr5: 43,484,268-43,487,021 TMEM267, C5orf34, 1 more genes
    nsv5842731copy number variation1nstd209human GRCh38 chr5: 43,484,122-43,486,496 , GRCh37.p13 chr5: 43,484,224-43,486,598 TMEM267, C5orf34, 1 more genes
    nsv5842431copy number variation1nstd209human GRCh38 chr5: 43,479,055-43,482,271 , GRCh37.p13 chr5: 43,479,157-43,482,373 C5orf34-AS1, TMEM267
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5469380copy number variation1nstd206human GRCh38 chr5: 43,479,000-43,482,326 , GRCh37.p13 chr5: 43,479,102-43,482,428 TMEM267, C5orf34-AS1
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5318683copy number variation1nstd204human GRCh37.p13 chr5: 43,479,099-43,482,430 , GRCh38.p13 chr5: 43,478,997-43,482,328 C5orf34-AS1, TMEM267
    nsv5226630copy number variation1nstd204human GRCh38.p13 chr5: 43,479,001-43,482,300 , GRCh37.p13 chr5: 43,479,103-43,482,402 C5orf34-AS1, TMEM267
    nsv5199745mobile element insertion1nstd203human GRCh38 chr5: 43,479,730-43,479,744 , GRCh37.p13 chr5: 43,479,832-43,479,846 TMEM267
    nsv5095668mobile element insertion1nstd203human GRCh38 chr5: 43,463,882-43,463,897 , GRCh37.p13 chr5: 43,463,984-43,463,999 TMEM267
    nsv4946905copy number variation1nstd200human GRCh38 chr5: 43,481,764-43,482,376 , GRCh37.p13 chr5: 43,481,866-43,482,478 C5orf34-AS1, TMEM267
    nsv4946904copy number variation1nstd200human GRCh38 chr5: 43,479,000-43,482,326 , GRCh37.p13 chr5: 43,479,102-43,482,428 TMEM267, C5orf34-AS1
    nsv4802715copy number variation1nstd200human GRCh37 chr5: 43,481,866-43,482,478 , GRCh38.p12 chr5: 43,481,764-43,482,376 TMEM267, C5orf34-AS1
    nsv4802714copy number variation1nstd200human GRCh37 chr5: 43,479,102-43,482,428 , GRCh38.p12 chr5: 43,479,000-43,482,326 TMEM267, C5orf34-AS1
    nsv4802713copy number variation1nstd200human GRCh37 chr5: 43,458,060-43,458,248 , GRCh38.p12 chr5: 43,457,958-43,458,146 TMEM267
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4662332copy number variation1nstd186human GRCh37 chr5: 43,479,102-43,482,428 , GRCh38.p12 chr5: 43,479,000-43,482,326 TMEM267, C5orf34-AS1
    nsv4598122copy number variation1nstd183human GRCh37 chr5: 43,479,102-43,482,428 , GRCh38.p12 chr5: 43,479,000-43,482,326 C5orf34-AS1, TMEM267
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