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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5594926copy number variation1nstd207human GRCh38 chr20: 19,248,672-19,251,475 , GRCh37.p13 chr20: 19,229,316-19,232,119 SLC24A3, SLC24A3-AS1
    nsv5526276copy number variation1nstd206human GRCh38 chr20: 19,264,640-19,267,815 , GRCh37.p13 chr20: 19,245,284-19,248,459 SLC24A3-AS1, SLC24A3
    nsv5519623copy number variation1nstd206human GRCh38 chr20: 19,262,913-19,262,981 , GRCh37.p13 chr20: 19,243,557-19,243,625 SLC24A3, SLC24A3-AS1
    nsv5517372copy number variation1nstd206human GRCh38 chr20: 19,248,673-19,251,476 , GRCh37.p13 chr20: 19,229,317-19,232,120 SLC24A3, SLC24A3-AS1
    nsv5326550copy number variation1nstd204human GRCh37.p13 chr20: 19,229,307-19,232,121 , GRCh38.p13 chr20: 19,248,663-19,251,477 SLC24A3, SLC24A3-AS1
    nsv5294980copy number variation1nstd204human GRCh38.p13 chr20: 19,249,115-19,251,489 , GRCh37.p13 chr20: 19,229,759-19,232,133 SLC24A3-AS1, SLC24A3
    nsv5160666mobile element insertion1nstd203human GRCh38 chr20: 19,266,389-19,266,406 , GRCh37.p13 chr20: 19,247,033-19,247,050 SLC24A3-AS1, SLC24A3
    nsv5025183copy number variation1nstd200human GRCh38 chr20: 19,185,203-19,443,483 , GRCh37.p13 chr20: 19,165,847-19,424,127 LOC101929547, SLC24A3-AS1, 1 more genes
    nsv5021610copy number variation1nstd200human GRCh38 chr20: 19,266,919-19,267,819 , GRCh37.p13 chr20: 19,247,563-19,248,463 SLC24A3-AS1, SLC24A3
    nsv5021609copy number variation1nstd200human GRCh38 chr20: 19,264,639-19,267,816 , GRCh37.p13 chr20: 19,245,283-19,248,460 SLC24A3, SLC24A3-AS1
    nsv5021608copy number variation1nstd200human GRCh38 chr20: 19,248,673-19,251,476 , GRCh37.p13 chr20: 19,229,317-19,232,120 SLC24A3-AS1, SLC24A3
    nsv4862257copy number variation1nstd200human GRCh37 chr20: 19,245,280-19,248,459 , GRCh38.p12 chr20: 19,264,636-19,267,815 SLC24A3, SLC24A3-AS1
    nsv4862256copy number variation1nstd200human GRCh37 chr20: 19,229,317-19,232,120 , GRCh38.p12 chr20: 19,248,673-19,251,476 SLC24A3-AS1, SLC24A3
    nsv4738683copy number variation1nstd199human GRCh37 chr20: 19,254,860-19,254,966 , GRCh38.p12 chr20: 19,274,216-19,274,322 SLC24A3, SLC24A3-AS1
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4628363copy number variation1nstd183human GRCh37 chr20: 19,229,311-19,232,116 , GRCh38.p12 chr20: 19,248,667-19,251,472 SLC24A3, SLC24A3-AS1
    nsv4392498copy number variation1nstd171human GRCh37 chr20: 19,254,468-19,254,900 , GRCh38.p12 chr20: 19,273,824-19,274,256 SLC24A3, SLC24A3-AS1
    nsv4392497copy number variation1nstd171human GRCh37 chr20: 19,254,448-19,254,880 , GRCh38.p12 chr20: 19,273,804-19,274,236 SLC24A3, SLC24A3-AS1
    nsv4392496copy number variation1nstd171human GRCh37 chr20: 19,239,970-19,240,002 , GRCh38.p12 chr20: 19,259,326-19,259,358 SLC24A3, SLC24A3-AS1
    nsv4350090copy number variation1nstd102humanPathogenic GRCh37 chr20: 11,716,825-19,331,055 , GRCh38.p12 chr20: 11,736,177-19,350,411 ENSAP1, BANF2, 107 more genes
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