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Items: 1 to 20 of 1442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956236insertion1nstd209human GRCh38 chr9: 41,934,122-41,934,122 , GRCh37.p13 chr9: 43,880,267-43,880,267 CNTNAP3B
    nsv5926889copy number variation1nstd209human GRCh38 chr9: 41,916,231-41,916,455 , GRCh37.p13 chr9: 43,897,934-43,898,158 CNTNAP3B
    nsv5919666copy number variation1nstd209human GRCh38 chr9: 42,030,764-42,030,814 , GRCh37.p13 chr9: 43,783,575-43,783,625 CNTNAP3B
    nsv5911060copy number variation1nstd209human GRCh38 chr9: 40,229,279-42,858,473 , GRCh37.p13 chr9: 42,792,885-46,287,854 , LOC107984035, 69 more genes
    nsv5909117copy number variation1nstd209human GRCh38 chr9: 40,903,761-43,206,180 , GRCh37.p13 chr9: 40,029,241-41,240,039 , LOC100420440, 62 more genes
    nsv5861928copy number variation2nstd209human GRCh38 chr9: 42,109,886-42,128,522 , GRCh37.p13 chr9: 43,685,867-43,704,503 CNTNAP3B
    nsv5859632copy number variation2nstd209human GRCh38 chr9: 42,129,850-42,136,274 , GRCh37.p13 chr9: 43,678,115-43,684,539 CNTNAP3B
    nsv5857358copy number variation2nstd209human GRCh38 chr9: 42,093,795-42,098,230 , GRCh37.p13 chr9: 43,716,159-43,720,594 LOC100420440, CNTNAP3B
    nsv5855909copy number variation2nstd209human GRCh38 chr9: 42,129,849-42,132,621 , GRCh37.p13 chr9: 43,681,768-43,684,540 CNTNAP3B
    nsv5852234copy number variation2nstd209human GRCh38 chr9: 42,123,636-42,132,621 , GRCh37.p13 chr9: 43,681,768-43,690,753 CNTNAP3B
    nsv5664563inversion1nstd207human GRCh38 chr9: 39,265,868-42,796,744 , GRCh37.p13 chr9: 42,792,885-46,287,854 , PTGER4P1, 95 more genes
    nsv5602911copy number variation1nstd207human GRCh38 chr9: 42,118,830-42,118,922 , GRCh37.p13 chr9: 43,695,467-43,695,559 CNTNAP3B
    nsv5598598copy number variation1nstd207human GRCh38 chr9: 42,118,832-42,119,134 , GRCh37.p13 chr9: 43,695,255-43,695,557 CNTNAP3B
    nsv5584730copy number variation1nstd207human GRCh38 chr9: 42,127,138-42,127,344 , GRCh37.p13 chr9: 43,687,045-43,687,251 CNTNAP3B
    nsv5554508sequence alteration1nstd206human GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104 , PTGER4P2, 168 more genes
    nsv5544110insertion1nstd206human GRCh38 chr9: 41,978,740-41,978,745 , GRCh37.p13 chr9: 43,835,644-43,835,649 CNTNAP3B
    nsv5259984copy number variation1nstd204human GRCh38.p13 chr9: 41,983,301-41,984,100 , GRCh37.p13 chr9: 43,830,289-43,831,088 CNTNAP3B
    nsv5259727copy number variation1nstd204human GRCh38.p13 chr9: 42,016,501-42,037,600 , GRCh37.p13 chr9: 43,776,789-43,797,888 CNTNAP3B
    nsv5259713copy number variation1nstd204human GRCh38.p13 chr9: 41,912,801-41,928,700 , GRCh37.p13 chr9: 43,885,689-43,901,588 CNTNAP3B
    nsv5259571copy number variation1nstd204human GRCh38.p13 chr9: 41,929,801-41,938,100 , GRCh37.p13 chr9: 43,876,289-43,884,588 CNTNAP3B
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