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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979509insertion1nstd209human GRCh38 chr16: 20,766,305-20,766,305 , GRCh37.p13 chr16: 20,777,627-20,777,627 ACSM3
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5945154copy number variation1nstd209human GRCh38 chr16: 20,793,141-20,794,742 , GRCh37.p13 chr16: 20,804,463-20,806,064 ACSM3, ERI2
    nsv5937422copy number variation1nstd209human GRCh38 chr16: 20,767,219-20,767,538 , GRCh37.p13 chr16: 20,778,541-20,778,860 ACSM3
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5884470copy number variation1nstd209human GRCh38 chr16: 20,793,119-20,794,768 , GRCh37.p13 chr16: 20,804,441-20,806,090 ACSM3, ERI2
    nsv5703991mobile element insertion2nstd211human GRCh38 chr16: 20,766,322-20,766,322 , GRCh37.p13 chr16: 20,777,644-20,777,644 ACSM3
    nsv5696146mobile element insertion1nstd211human GRCh38 chr16: 20,742,813-20,742,813 , GRCh37.p13 chr16: 20,754,135-20,754,135 ACSM3
    nsv5664135insertion1nstd207human GRCh38 chr16: 20,766,305-20,766,305 , GRCh37.p13 chr16: 20,777,627-20,777,627 ACSM3
    nsv5594037copy number variation1nstd207human GRCh38 chr16: 20,767,219-20,767,538 , GRCh37.p13 chr16: 20,778,541-20,778,860 ACSM3
    nsv5553771insertion1nstd206human GRCh38 chr16: 20,766,305-20,766,305 , GRCh37.p13 chr16: 20,777,627-20,777,627 ACSM3
    nsv5526308copy number variation1nstd206human GRCh38 chr16: 20,763,354-20,764,295 , GRCh37.p13 chr16: 20,774,676-20,775,617 ACSM3
    nsv5515318copy number variation1nstd206human GRCh38 chr16: 20,767,235-20,767,539 , GRCh37.p13 chr16: 20,778,557-20,778,861 ACSM3
    nsv5383979mobile element deletion2nstd186human GRCh37 chr16: 20,778,557-20,778,861 , GRCh38.p12 chr16: 20,767,235-20,767,539 ACSM3
    nsv5205838mobile element deletion1nstd204human GRCh38.p13 chr16: 20,767,235-20,767,539 , GRCh37.p13 chr16: 20,778,557-20,778,861 ACSM3
    nsv5158395mobile element insertion1nstd203human GRCh38 chr16: 20,766,305-20,766,322 , GRCh37.p13 chr16: 20,777,627-20,777,644 ACSM3
    nsv5153663mobile element insertion1nstd203human GRCh38 chr16: 20,766,312-20,766,322 , GRCh37.p13 chr16: 20,777,634-20,777,644 ACSM3
    nsv5149176mobile element insertion1nstd203human GRCh38 chr16: 20,766,308-20,766,322 , GRCh37.p13 chr16: 20,777,630-20,777,644 ACSM3
    nsv5147590mobile element insertion1nstd203human GRCh38 chr16: 20,766,307-20,766,322 , GRCh37.p13 chr16: 20,777,629-20,777,644 ACSM3
    nsv5145796mobile element insertion1nstd203human GRCh38 chr16: 20,766,304-20,766,322 , GRCh37.p13 chr16: 20,777,626-20,777,644 ACSM3
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