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Items: 1 to 20 of 308

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968000inversion1nstd209human GRCh38 chr22: 23,676,272-24,601,321 , GRCh37.p13 chr22: 24,018,459-24,997,288 , ADORA2A, 38 more genes
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5949708copy number variation1nstd209human GRCh38 chr22: 24,527,969-24,537,238 , GRCh37.p13 chr22: 24,923,937-24,933,206 UPB1
    nsv5882378copy number variation1nstd209human GRCh38 chr22: 24,527,937-24,536,766 , GRCh37.p13 chr22: 24,923,905-24,932,734 UPB1
    nsv5537601copy number variation1nstd206human GRCh38 chr22: 24,528,065-24,537,258 , GRCh37.p13 chr22: 24,924,033-24,933,226 UPB1
    nsv5381153copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,915,453-24,921,762 , GRCh38.p12 chr22: 23,573,266-24,525,794 GSTT2B, SUSD2, 37 more genes
    nsv5381087copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,699,269-24,992,266 , GRCh38.p12 chr22: 23,357,082-24,596,299 LOC100129358, VPREB3, 49 more genes
    nsv5360442translocation1nstd200human GRCh38 chr22: 24,499,929-24,499,929 , GRCh38 chr22: 24,499,801-24,499,801 , GRCh37.p13 chr22: 24,895,769-24,895,769 , GRCh37.p13 chr22: 24,895,897-24,895,897 UPB1
    nsv5322608copy number variation1nstd204human GRCh38.p13 chr22: 24,527,782-24,537,449 , GRCh37.p13 chr22: 24,923,750-24,933,417 UPB1
    nsv5295010copy number variation1nstd204human GRCh38.p13 chr22: 24,511,925-24,523,424 , GRCh37.p13 chr22: 24,907,893-24,919,392 UPB1
    nsv5291389copy number variation1nstd204human GRCh38.p13 chr22: 24,528,001-24,538,600 , GRCh37.p13 chr22: 24,923,969-24,934,568 UPB1, GUCD1
    nsv5285189copy number variation1nstd204human GRCh38.p13 chr22: 24,527,375-24,537,153 , GRCh37.p13 chr22: 24,923,343-24,933,121 UPB1
    nsv5175614mobile element insertion1nstd203human GRCh38 chr22: 24,513,735-24,513,742 , GRCh37.p13 chr22: 24,909,703-24,909,710 UPB1
    nsv5032913copy number variation1nstd200human GRCh38 chr22: 24,513,589-24,514,911 , GRCh37.p13 chr22: 24,909,557-24,910,879 UPB1
    nsv5032872copy number variation1nstd200human GRCh38 chr22: 24,527,927-24,537,264 , GRCh37.p13 chr22: 24,923,895-24,933,232 UPB1
    nsv4869213copy number variation1nstd200human GRCh37 chr22: 24,909,557-24,910,879 , GRCh38.p12 chr22: 24,513,589-24,514,911 UPB1
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4729959copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,650,873-25,043,046 , GRCh38.p12 chr22: 23,308,686-24,647,079 BCRP1, SNRPD3, 55 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
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