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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146541copy number variation1nstd232human GRCh37.p13 chr3: 52,727,344-52,727,421 , GRCh38.p12 chr3: 52,693,328-52,693,405 GNL3, GLT8D1
    nsv7145820copy number variation1nstd232human GRCh37.p13 chr3: 52,727,558-52,727,644 , GRCh38.p12 chr3: 52,693,542-52,693,628 GNL3, GLT8D1
    nsv7142335insertion1nstd232human GRCh37.p13 chr3: 52,727,824-52,727,824 , GRCh38.p12 chr3: 52,693,808-52,693,808 GNL3, GLT8D1
    nsv7141830insertion1nstd232human GRCh37.p13 chr3: 52,727,066-52,727,066 , GRCh38.p12 chr3: 52,693,050-52,693,050 GNL3, GLT8D1, 1 more genes
    nsv7141050insertion1nstd232human GRCh37.p13 chr3: 52,740,299-52,740,299 , GRCh38.p12 chr3: 52,706,283-52,706,283 SPCS1, GLT8D1
    nsv7140594insertion1nstd232human GRCh37.p13 chr3: 52,730,946-52,730,946 , GRCh38.p12 chr3: 52,696,930-52,696,930 GLT8D1
    nsv7137540copy number variation1nstd232human GRCh37.p13 chr3: 52,728,117-52,728,205 , GRCh38.p12 chr3: 52,694,101-52,694,189 GNL3, GLT8D1
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7041270inversion1nstd229human GRCh38 chr3: 52,619,221-53,173,329 , GRCh37.p13 chr3: 52,653,237-53,185,061 SNORD19, SNORD19C, 23 more genes
    nsv6717956copy number variation1nstd229human GRCh38 chr3: 52,650,204-52,702,405 , GRCh37.p13 chr3: 52,684,220-52,736,421 SNORD19B, GLT8D1, 6 more genes
    nsv6716874copy number variation1nstd229human GRCh38 chr3: 52,619,220-52,838,314 , GRCh37.p13 chr3: 52,653,236-52,872,330 ITIH4-AS1, STIMATE, 18 more genes
    nsv6715302copy number variation1nstd229human GRCh38 chr3: 52,656,401-52,872,900 , GRCh37.p13 chr3: 52,690,417-52,906,916 SNORD136, GLT8D1, 19 more genes
    nsv6539894inversion1nstd223human GRCh38 chr3: 52,698,555-52,699,388 , GRCh37.p13 chr3: 52,732,571-52,733,404 GLT8D1
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6283900insertion4nstd214human GRCh38 chr3: 52,696,930-52,696,930 , GRCh37.p13 chr3: 52,730,946-52,730,946 GLT8D1
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv6078125insertion1nstd212human GRCh38 chr3: 52,696,930-52,696,930 , GRCh37.p13 chr3: 52,730,946-52,730,946 GLT8D1
    nsv5965210insertion1nstd209human GRCh38 chr3: 52,696,930-52,696,930 , GRCh37.p13 chr3: 52,730,946-52,730,946 GLT8D1
    nsv5678216mobile element insertion1nstd211human GRCh38 chr3: 52,703,817-52,703,817 , GRCh37.p13 chr3: 52,737,833-52,737,833 GLT8D1
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