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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940308copy number variation1nstd209human GRCh38 chr20: 2,224,825-2,385,105 , GRCh37.p13 chr20: 2,205,471-2,365,751 LOC105372503, TGM3, 1 more genes
    nsv5871933copy number variation1nstd209human GRCh38 chr20: 2,299,146-2,319,090 , GRCh37.p13 chr20: 2,279,792-2,299,736 TGM3, LOC105372503
    nsv5871245copy number variation1nstd209human GRCh38 chr20: 2,326,141-2,328,234 , GRCh37.p13 chr20: 2,306,787-2,308,880 TGM3
    nsv5869439copy number variation2nstd209human GRCh38 chr20: 2,338,160-2,343,199 , GRCh37.p13 chr20: 2,318,806-2,323,845 TGM3
    nsv5702103mobile element insertion1nstd211human GRCh38 chr20: 2,295,687-2,295,687 , GRCh37.p13 chr20: 2,276,333-2,276,333 LOC105372503, TGM3
    nsv5659966insertion1nstd207human GRCh38 chr20: 2,334,212-2,334,212 , GRCh37.p13 chr20: 2,314,858-2,314,858 TGM3
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5522313copy number variation1nstd206human GRCh38 chr20: 2,224,825-2,385,108 , GRCh37.p13 chr20: 2,205,471-2,365,754 LOC105372503, TGM3, 1 more genes
    nsv5424131mobile element insertion1nstd206human GRCh38 chr20: 2,295,687-2,295,738 , GRCh37.p13 chr20: 2,276,333-2,276,384 LOC105372503, TGM3
    nsv5324521copy number variation1nstd204human GRCh38.p13 chr20: 2,303,308-2,312,369 , GRCh37.p13 chr20: 2,283,954-2,293,015 TGM3
    nsv5288428copy number variation1nstd204human GRCh38.p13 chr20: 2,304,871-2,312,379 , GRCh37.p13 chr20: 2,285,517-2,293,025 TGM3
    nsv5028389copy number variation1nstd200human GRCh38 chr20: 2,322,157-2,323,299 , GRCh37.p13 chr20: 2,302,803-2,303,945 TGM3
    nsv5028388copy number variation1nstd200human GRCh38 chr20: 2,308,129-2,310,791 , GRCh37.p13 chr20: 2,288,775-2,291,437 TGM3
    nsv5025058copy number variation1nstd200human GRCh38 chr20: 2,056,134-2,737,157 , GRCh37.p13 chr20: 2,036,780-2,717,803 , LOC105372507, 22 more genes
    nsv4861649copy number variation1nstd200human GRCh37 chr20: 2,302,803-2,303,945 , GRCh38.p12 chr20: 2,322,157-2,323,299 TGM3
    nsv4861648copy number variation1nstd200human GRCh37 chr20: 2,283,964-2,293,008 , GRCh38.p12 chr20: 2,303,318-2,312,362 TGM3
    nsv4627971copy number variation1nstd183human GRCh37 chr20: 2,308,307-2,317,490 , GRCh38.p12 chr20: 2,327,661-2,336,844 TGM3
    nsv4577752mobile element insertion1nstd166human GRCh37.p13 chr20: 2,286,920-2,286,920 , GRCh38.p12 chr20: 2,306,274-2,306,274 TGM3
    nsv4560694insertion1nstd166human GRCh37.p13 chr20: 2,276,320-2,276,320 , GRCh38.p12 chr20: 2,295,674-2,295,674 LOC105372503, TGM3
    nsv4536889copy number variation1nstd166human GRCh37.p13 chr20: 2,205,471-2,365,754 , GRCh38.p12 chr20: 2,224,825-2,385,108 TGM6, TGM3, 1 more genes
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