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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916020copy number variation1nstd209human GRCh38 chr10: 5,423,418-5,424,800 , GRCh37.p13 chr10: 5,465,381-5,466,763 NET1
    nsv5853121copy number variation1nstd209human GRCh38 chr10: 5,423,464-5,424,863 , GRCh37.p13 chr10: 5,465,427-5,466,826 NET1
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv5476121copy number variation1nstd206human GRCh38 chr10: 5,423,420-5,424,801 , GRCh37.p13 chr10: 5,465,383-5,466,764 NET1
    nsv5248179copy number variation1nstd204human GRCh38.p13 chr10: 5,459,151-5,529,793 , GRCh37.p13 chr10: 5,501,114-5,571,756 , CALML5, 3 more genes
    nsv5134185mobile element insertion1nstd203human GRCh38 chr10: 5,450,552-5,450,562 , GRCh37.p13 chr10: 5,492,515-5,492,525 NET1
    nsv4973522copy number variation1nstd200human GRCh38 chr10: 5,424,804-5,467,522 , GRCh37.p13 chr10: 5,466,767-5,509,485 NET1
    nsv4841477copy number variation1nstd200human GRCh37 chr10: 5,465,383-5,466,764 , GRCh38.p12 chr10: 5,423,420-5,424,801 NET1
    nsv4831282copy number variation1nstd200human GRCh37 chr10: 5,466,767-5,509,485 , GRCh38.p12 chr10: 5,424,804-5,467,522 NET1
    nsv4714255copy number variation1nstd195human GRCh37 chr10: 5,456,151-5,763,601 , GRCh38.p12 chr10: 5,414,188-5,721,638 , ASB13, 12 more genes
    nsv4675507copy number variation1nstd102humanUncertain significance GRCh37 chr10: 5,201,443-5,658,539 , GRCh38.p12 chr10: 5,159,245-5,616,576 LASTR, LINC02561, 15 more genes
    nsv4493773mobile element insertion1nstd166human GRCh37.p13 chr10: 5,492,536-5,492,536 , GRCh38.p12 chr10: 5,450,573-5,450,573 NET1
    nsv4479769mobile element insertion1nstd166human GRCh37.p13 chr10: 5,492,511-5,492,511 , GRCh38.p12 chr10: 5,450,548-5,450,548 NET1
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4419413copy number variation1nstd174human GRCh37 chr10: 5,465,388-5,466,835 , GRCh38.p12 chr10: 5,423,425-5,424,872 NET1
    nsv4191998copy number variation1nstd166human GRCh37.p13 chr10: 5,465,383-5,466,764 , GRCh38.p12 chr10: 5,423,420-5,424,801 NET1
    nsv4189114copy number variation1nstd166human GRCh37.p13 chr10: 5,496,485-5,496,910 , GRCh38.p12 chr10: 5,454,522-5,454,947 NET1
    nsv4184651copy number variation1nstd166human GRCh37.p13 chr10: 5,494,489-5,494,818 , GRCh38.p12 chr10: 5,452,526-5,452,855 NET1
    nsv4183930copy number variation1nstd166human GRCh37.p13 chr10: 5,494,884-5,495,210 , GRCh38.p12 chr10: 5,452,921-5,453,247 NET1
    nsv4183404copy number variation1nstd166human GRCh37.p13 chr10: 5,485,832-5,486,153 , GRCh38.p12 chr10: 5,443,869-5,444,190 NET1
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