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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5719879mobile element insertion1nstd211human GRCh38 chr16: 23,412,463-23,412,463 , GRCh37.p13 chr16: 23,423,784-23,423,784 RN7SKP23, COG7
    nsv5662251insertion1nstd207human GRCh38 chr16: 23,408,132-23,408,132 , GRCh37.p13 chr16: 23,419,453-23,419,453 COG7
    nsv5593499copy number variation1nstd207human GRCh38 chr16: 23,439,135-23,439,280 , GRCh37.p13 chr16: 23,450,456-23,450,601 COG7
    nsv5591447copy number variation1nstd207human GRCh38 chr16: 23,408,151-23,408,459 , GRCh37.p13 chr16: 23,419,472-23,419,780 COG7
    nsv5313130copy number variation1nstd204human GRCh38.p13 chr16: 23,428,796-23,429,286 , GRCh37.p13 chr16: 23,440,117-23,440,607 COG7
    nsv5266082copy number variation1nstd204human GRCh38.p13 chr16: 23,390,301-23,477,900 , GRCh37.p13 chr16: 23,401,622-23,489,221 GGA2, RN7SKP23, 1 more genes
    nsv5003195copy number variation1nstd200human GRCh38 chr16: 23,444,623-23,444,726 , GRCh37.p13 chr16: 23,455,944-23,456,047 COG7
    nsv4994556copy number variation1nstd200human GRCh38 chr16: 23,447,578-23,515,419 , GRCh37.p13 chr16: 23,458,899-23,526,740 GGA2, CCNYL7, 1 more genes
    nsv4994555copy number variation1nstd200human GRCh38 chr16: 23,385,269-23,393,891 , GRCh37.p13 chr16: 23,396,590-23,405,212 COG7
    nsv4864063copy number variation1nstd200human GRCh37 chr16: 23,458,899-23,526,740 , GRCh38.p12 chr16: 23,447,578-23,515,419 CCNYL7, COG7, 1 more genes
    nsv4864062copy number variation1nstd200human GRCh37 chr16: 23,396,590-23,405,209 , GRCh38.p12 chr16: 23,385,269-23,393,888 COG7
    nsv4850734copy number variation1nstd200human GRCh37 chr16: 23,450,316-23,452,670 , GRCh38.p12 chr16: 23,438,995-23,441,349 COG7
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
    nsv4675970copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,802-29,351,826 , GRCh38.p12 chr16: 21,565,481-29,340,505 NSMCE1, LOC105371149, 152 more genes
    nsv4575565mobile element insertion1nstd166human GRCh37.p13 chr16: 23,423,767-23,423,767 , GRCh38.p12 chr16: 23,412,446-23,412,446 COG7, RN7SKP23
    nsv4504827mobile element insertion1nstd166human GRCh37.p13 chr16: 23,429,241-23,429,241 , GRCh38.p12 chr16: 23,417,920-23,417,920 COG7
    nsv4504564mobile element insertion1nstd166human GRCh37.p13 chr16: 23,420,024-23,420,024 , GRCh38.p12 chr16: 23,408,703-23,408,703 COG7
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