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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5958164copy number variation1nstd209human GRCh38 chr20: 62,954,095-62,954,147 , GRCh37.p13 chr20: 61,585,447-61,585,499 SLC17A9
    nsv5951075copy number variation1nstd209human GRCh38 chr20: 62,957,051-62,957,126 , GRCh37.p13 chr20: 61,588,403-61,588,478 SLC17A9
    nsv5666493insertion1nstd207human GRCh38 chr20: 62,960,987-62,960,987 , GRCh37.p13 chr20: 61,592,339-61,592,339 SLC17A9
    nsv5666127insertion1nstd207human GRCh38 chr20: 62,966,030-62,966,030 , GRCh37.p13 chr20: 61,597,382-61,597,382 SLC17A9
    nsv5600892copy number variation1nstd207human GRCh38 chr20: 62,960,990-62,961,069 , GRCh37.p13 chr20: 61,592,342-61,592,421 SLC17A9
    nsv5597275copy number variation1nstd207human GRCh38 chr20: 62,966,085-62,966,249 , GRCh37.p13 chr20: 61,597,437-61,597,601 SLC17A9
    nsv5596504copy number variation1nstd207human GRCh38 chr20: 62,966,030-62,966,084 , GRCh37.p13 chr20: 61,597,382-61,597,436 SLC17A9
    nsv5595622copy number variation1nstd207human GRCh38 chr20: 62,957,819-62,957,872 , GRCh37.p13 chr20: 61,589,171-61,589,224 SLC17A9
    nsv5587932copy number variation1nstd207human GRCh38 chr20: 62,957,051-62,957,126 , GRCh37.p13 chr20: 61,588,403-61,588,478 SLC17A9
    nsv5586179copy number variation1nstd207human GRCh38 chr20: 62,954,025-62,954,077 , GRCh37.p13 chr20: 61,585,377-61,585,429 SLC17A9
    nsv5586093copy number variation1nstd207human GRCh38 chr20: 62,960,987-62,961,226 , GRCh37.p13 chr20: 61,592,339-61,592,578 SLC17A9
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    nsv5526750copy number variation1nstd206human GRCh38 chr20: 62,957,309-62,958,458 , GRCh37.p13 chr20: 61,588,661-61,589,810 SLC17A9
    nsv5391016copy number variation1nstd186human GRCh37 chr20: 61,597,413-61,597,663 , GRCh38.p12 chr20: 62,966,061-62,966,311 SLC17A9
    nsv5390744copy number variation1nstd186human GRCh37 chr20: 61,592,390-61,592,699 , GRCh38.p12 chr20: 62,961,038-62,961,347 SLC17A9
    nsv5381809copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,510,452-62,315,381 , GRCh38.p12 chr20: 62,879,100-63,684,028 MIR3196, NKAIN4, 40 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5350557translocation1nstd200human GRCh38 chr20: 62,960,643-62,960,643 , GRCh38 chr20: 62,960,704-62,960,704 , GRCh37.p13 chr20: 61,591,995-61,591,995 , GRCh37.p13 chr20: 61,592,056-61,592,056 SLC17A9
    nsv5340931translocation1nstd200human GRCh37 chr20: 61,592,056-61,592,056 , GRCh37 chr20: 61,591,995-61,591,995 , GRCh38.p12 chr20: 62,960,643-62,960,643 , GRCh38.p12 chr20: 62,960,704-62,960,704 SLC17A9
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