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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7034779copy number variation1nstd229human GRCh38 chr20: 45,830,357-45,833,968 , GRCh37.p13 chr20: 44,458,996-44,462,607 TNNC2, SNX21
    nsv7023025copy number variation1nstd229human GRCh38 chr20: 45,780,618-45,847,012 , GRCh37.p13 chr20: 44,409,257-44,475,651 UBE2C, SNX21, 4 more genes
    nsv7020478copy number variation1nstd229human GRCh38 chr20: 45,816,899-45,824,574 , GRCh37.p13 chr20: 44,445,538-44,453,213 TNNC2, UBE2C
    nsv6538106copy number variation1nstd223human GRCh38 chr20: 45,830,357-45,833,965 , GRCh37.p13 chr20: 44,458,996-44,462,604 SNX21, TNNC2
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6146432copy number variation1nstd206human GRCh38 chr20: 45,816,625-45,822,625 , GRCh37.p13 chr20: 44,445,264-44,451,264 TNNC2, UBE2C
    nsv6134165copy number variation1nstd213human GRCh37 chr20: 44,320,000-45,430,001 , GRCh38.p12 chr20: 45,691,361-46,801,362 MMP9, MKRN7P, 39 more genes
    nsv6133816copy number variation1nstd213human GRCh37 chr20: 43,650,000-45,170,001 , GRCh38.p12 chr20: 45,021,359-46,541,362 MMP9, PI3, 76 more genes
    nsv5957522copy number variation1nstd209human GRCh38 chr20: 45,828,871-45,829,049 , GRCh37.p13 chr20: 44,457,510-44,457,688 TNNC2
    nsv5297245copy number variation1nstd204human GRCh38.p13 chr20: 45,815,905-45,822,006 , GRCh37.p13 chr20: 44,444,544-44,450,645 TNNC2, UBE2C
    nsv5025646copy number variation1nstd200human GRCh38 chr20: 45,780,618-45,847,012 , GRCh37.p13 chr20: 44,409,257-44,475,651 TNNC2, UBE2C, 4 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4573726mobile element insertion1nstd166human GRCh37.p13 chr20: 44,458,579-44,458,579 , GRCh38.p12 chr20: 45,829,940-45,829,940 TNNC2
    nsv4502023mobile element insertion1nstd166human GRCh37.p13 chr20: 44,457,162-44,457,162 , GRCh38.p12 chr20: 45,828,523-45,828,523 TNNC2
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 more genes
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