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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146514copy number variation1nstd232human GRCh37.p13 chr14: 89,977,571-89,977,629 , GRCh38.p12 chr14: 89,511,227-89,511,285 FOXN3
    nsv7145429copy number variation1nstd232human GRCh37.p13 chr14: 89,827,079-89,827,137 , GRCh38.p12 chr14: 89,360,735-89,360,793 FOXN3, LOC101928817
    nsv7144862copy number variation1nstd232human GRCh37.p13 chr14: 89,977,476-89,977,533 , GRCh38.p12 chr14: 89,511,132-89,511,189 FOXN3
    nsv7143264copy number variation1nstd232human GRCh37.p13 chr14: 89,977,480-89,977,581 , GRCh38.p12 chr14: 89,511,136-89,511,237 FOXN3
    nsv7138583insertion1nstd232human GRCh37.p13 chr14: 89,827,042-89,827,042 , GRCh38.p12 chr14: 89,360,698-89,360,698 FOXN3, LOC101928817
    nsv7137608copy number variation1nstd232human GRCh37.p13 chr14: 89,972,456-89,972,533 , GRCh38.p12 chr14: 89,506,112-89,506,189 FOXN3
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 LOC100128939, FAM181A-AS1, 104 more genes
    nsv7069406inversion1nstd229human GRCh38 chr14: 89,243,172-89,243,299 , GRCh37.p13 chr14: 89,709,516-89,709,643 FOXN3
    nsv7069334inversion1nstd229human GRCh38 chr14: 84,501,002-89,358,377 , GRCh37.p13 chr14: 84,967,346-89,824,721 EML5, LOC105370612, 35 more genes
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7063776inversion1nstd229human GRCh38 chr14: 89,569,426-89,576,159 , GRCh37.p13 chr14: 90,035,770-90,042,503 FOXN3, FOXN3-AS2
    nsv7059378inversion1nstd229human GRCh38 chr14: 87,626,566-93,230,083 , GRCh37.p13 chr14: 88,092,910-93,674,575 PSMC1, HISLA, 87 more genes
    nsv6977405copy number variation1nstd229human GRCh38 chr14: 89,281,613-89,283,547 , GRCh37.p13 chr14: 89,747,957-89,749,891 FOXN3
    nsv6976483copy number variation1nstd229human GRCh38 chr14: 89,602,956-89,611,962 , GRCh37.p13 chr14: 90,069,300-90,078,306 FOXN3
    nsv6975542copy number variation1nstd229human GRCh38 chr14: 89,291,781-89,296,663 , GRCh37.p13 chr14: 89,758,125-89,763,007 CAP2P1, FOXN3
    nsv6973975copy number variation1nstd229human GRCh38 chr14: 89,538,608-89,544,580 , GRCh37.p13 chr14: 90,004,952-90,010,924 FOXN3
    nsv6973575copy number variation1nstd229human GRCh38 chr14: 89,533,733-89,533,775 , GRCh37.p13 chr14: 90,000,077-90,000,119 FOXN3
    nsv6971950copy number variation1nstd229human GRCh38 chr14: 89,479,866-89,481,662 , GRCh37.p13 chr14: 89,946,210-89,948,006 FOXN3
    nsv6971898copy number variation1nstd229human GRCh38 chr14: 89,524,359-89,605,017 , GRCh37.p13 chr14: 89,990,703-90,071,361 FOXN3, FOXN3-AS2
    nsv6971595copy number variation1nstd229human GRCh38 chr14: 89,249,062-89,249,641 , GRCh37.p13 chr14: 89,715,406-89,715,985 FOXN3
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