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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966883copy number variation1nstd209human GRCh38 chr20: 31,606,543-31,608,451 , GRCh37.p13 chr20: 30,194,346-30,196,254 MIR3193, ID1
    nsv5882866copy number variation2nstd209human GRCh38 chr20: 31,603,952-31,608,751 , GRCh37.p13 chr20: 30,191,755-30,196,554 MIR3193, LOC105372588, 1 more genes
    nsv5873950copy number variation2nstd209human GRCh38 chr20: 31,606,502-31,608,501 , GRCh37.p13 chr20: 30,194,305-30,196,304 ID1, MIR3193
    nsv5871869copy number variation2nstd209human GRCh38 chr20: 31,605,452-31,608,751 , GRCh37.p13 chr20: 30,193,255-30,196,554 ID1, MIR3193, 1 more genes
    nsv5603877copy number variation1nstd207human GRCh38 chr20: 31,606,543-31,608,451 , GRCh37.p13 chr20: 30,194,346-30,196,254 ID1, MIR3193
    nsv5526739copy number variation1nstd206human GRCh38 chr20: 31,606,554-31,608,452 , GRCh37.p13 chr20: 30,194,357-30,196,255 MIR3193, ID1
    nsv5350284translocation1nstd200human GRCh38 chr20: 31,606,554-31,606,554 , GRCh38 chr20: 31,608,452-31,608,452 , GRCh37.p13 chr20: 30,196,255-30,196,255 , GRCh37.p13 chr20: 30,194,357-30,194,357 MIR3193, ID1
    nsv5329253copy number variation1nstd204human GRCh37.p13 chr20: 30,194,335-30,196,276 , GRCh38.p13 chr20: 31,606,532-31,608,473 ID1, MIR3193
    nsv5327306copy number variation1nstd204human GRCh38.p13 chr20: 31,579,574-31,619,257 , GRCh37.p13 chr20: 30,167,377-30,207,060 ID1, LOC105372588, 2 more genes
    nsv5295742copy number variation1nstd204human GRCh38.p13 chr20: 31,603,152-31,607,951 , GRCh37.p13 chr20: 30,190,955-30,195,754 ID1, MIR3193, 1 more genes
    nsv5294484copy number variation1nstd204human GRCh38.p13 chr20: 31,606,552-31,609,551 , GRCh37.p13 chr20: 30,194,355-30,197,354 MIR3193, ID1
    nsv5290173copy number variation1nstd204human GRCh38.p13 chr20: 31,580,301-31,617,600 , GRCh37.p13 chr20: 30,168,104-30,205,403 RNU6-384P, LOC105372588, 2 more genes
    nsv5286541copy number variation1nstd204human GRCh38.p13 chr20: 31,582,235-31,660,719 , GRCh37.p13 chr20: 30,170,038-30,248,522 ID1, LOC105372588, 2 more genes
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5281749copy number variation1nstd204human GRCh38.p13 chr20: 31,606,552-31,619,007 , GRCh37.p13 chr20: 30,194,355-30,206,810 ID1, MIR3193
    nsv5190165mobile element insertion1nstd203human GRCh38 chr20: 31,606,625-31,606,625 , GRCh37.p13 chr20: 30,194,428-30,194,428 MIR3193, ID1
    nsv5025506copy number variation1nstd200human GRCh38 chr20: 31,594,163-31,637,367 , GRCh37.p13 chr20: 30,181,966-30,225,170 ID1, MIR3193, 2 more genes
    nsv5025501copy number variation1nstd200human GRCh38 chr20: 31,308,012-31,715,091 , GRCh37.p13 chr20: 29,895,815-30,302,894 CD24P3, COX4I2, 24 more genes
    nsv4868563copy number variation1nstd200human GRCh37 chr20: 30,194,357-30,196,255 , GRCh38.p12 chr20: 31,606,554-31,608,452 ID1, MIR3193
    nsv4729837copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,833,534-30,494,851 , GRCh38.p12 chr20: 31,245,731-31,907,048 DEFB117, LOC105372588, 34 more genes
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