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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924082copy number variation1nstd209human GRCh38 chr10: 98,263,802-98,265,473 , GRCh37.p13 chr10: 100,023,559-100,025,230 LOXL4
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5585991copy number variation1nstd207human GRCh38 chr10: 98,265,361-98,265,695 , GRCh37.p13 chr10: 100,025,118-100,025,452 LOXL4
    nsv5477765copy number variation1nstd206human GRCh38 chr10: 98,265,379-98,265,696 , GRCh37.p13 chr10: 100,025,136-100,025,453 LOXL4
    nsv5387518copy number variation3nstd186human GRCh37 chr10: 100,025,136-100,025,453 , GRCh38.p12 chr10: 98,265,379-98,265,696 LOXL4
    nsv5307503copy number variation1nstd204human GRCh38.p13 chr10: 98,265,379-98,265,696 , GRCh37.p13 chr10: 100,025,136-100,025,453 LOXL4
    nsv5241114copy number variation1nstd204human GRCh38.p13 chr10: 98,265,401-98,265,700 , GRCh37.p13 chr10: 100,025,158-100,025,457 LOXL4
    nsv4970224copy number variation1nstd200human GRCh38 chr10: 98,265,379-98,265,696 , GRCh37.p13 chr10: 100,025,136-100,025,453 LOXL4
    nsv4970223copy number variation1nstd200human GRCh38 chr10: 98,263,823-98,265,474 , GRCh37.p13 chr10: 100,023,580-100,025,231 LOXL4
    nsv4970222copy number variation1nstd200human GRCh38 chr10: 98,262,773-98,271,224 , GRCh37.p13 chr10: 100,022,530-100,030,981 LOXL4
    nsv4842393copy number variation1nstd200human GRCh37 chr10: 100,022,530-100,030,981 , GRCh38.p12 chr10: 98,262,773-98,271,224 LOXL4
    nsv4840867copy number variation1nstd200human GRCh37 chr10: 100,025,136-100,025,453 , GRCh38.p12 chr10: 98,265,379-98,265,696 LOXL4
    nsv4837906copy number variation1nstd200human GRCh37 chr10: 100,023,580-100,025,231 , GRCh38.p12 chr10: 98,263,823-98,265,474 LOXL4
    nsv4740416copy number variation1nstd199human GRCh37 chr10: 100,025,129-100,025,463 , GRCh38.p12 chr10: 98,265,372-98,265,706 LOXL4
    nsv4729159copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,015,920-100,234,444 , GRCh38.p12 chr10: 98,256,163-98,474,687 LOXL4, HPS1-AS1, 6 more genes
    nsv4703841copy number variation1nstd195human GRCh37 chr10: 100,025,118-100,025,119 , GRCh38.p12 chr10: 98,265,361-98,265,362 LOXL4
    nsv4652487copy number variation1nstd186human GRCh37 chr10: 100,025,125-100,025,464 , GRCh38.p12 chr10: 98,265,368-98,265,707 LOXL4
    nsv4639232copy number variation1nstd186human GRCh37 chr10: 100,025,080-100,025,453 , GRCh38.p12 chr10: 98,265,323-98,265,696 LOXL4
    nsv4485938mobile element insertion1nstd166human GRCh37.p13 chr10: 100,020,169-100,020,169 , GRCh38.p12 chr10: 98,260,412-98,260,412 LOXL4
    nsv4418617copy number variation1nstd174human GRCh37 chr10: 100,025,093-100,025,492 , GRCh38.p12 chr10: 98,265,336-98,265,735 LOXL4
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