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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925701copy number variation1nstd209human GRCh38 chr8: 17,555,515-17,556,356 , GRCh37.p13 chr8: 17,413,024-17,413,865 SLC7A2
    nsv5918025copy number variation1nstd209human GRCh38 chr8: 17,522,461-17,532,944 , GRCh37.p13 chr8: 17,379,970-17,390,453 SLC7A2
    nsv5858984copy number variation1nstd209human GRCh38 chr8: 17,522,441-17,531,901 , GRCh37.p13 chr8: 17,379,950-17,389,410 SLC7A2
    nsv5727699mobile element insertion2nstd211human GRCh38 chr8: 17,561,265-17,561,265 , GRCh37.p13 chr8: 17,418,774-17,418,774 SLC7A2
    nsv5710128mobile element insertion2nstd211human GRCh38 chr8: 17,525,131-17,525,131 , GRCh37.p13 chr8: 17,382,640-17,382,640 SLC7A2
    nsv5569784copy number variation1nstd207human GRCh38 chr8: 17,552,512-17,552,597 , GRCh37.p13 chr8: 17,410,021-17,410,106 SLC7A2
    nsv5556022mobile element insertion1nstd206human GRCh38 chr8: 17,561,265-17,561,316 , GRCh37.p13 chr8: 17,418,774-17,418,825 SLC7A2
    nsv5493063copy number variation1nstd206human GRCh38 chr8: 17,490,010-17,737,534 , GRCh37.p13 chr8: 17,347,519-17,595,043 PDGFRL, SLC7A2, 3 more genes
    nsv5492142copy number variation1nstd206human GRCh38 chr8: 17,555,518-17,556,357 , GRCh37.p13 chr8: 17,413,027-17,413,866 SLC7A2
    nsv5396051mobile element insertion1nstd206human GRCh38 chr8: 17,525,131-17,525,182 , GRCh37.p13 chr8: 17,382,640-17,382,691 SLC7A2
    nsv5379077translocation1nstd200human GRCh38 chr8: 17,556,357-17,556,357 , GRCh38 chr8: 17,555,518-17,555,518 , GRCh37.p13 chr8: 17,413,866-17,413,866 , GRCh37.p13 chr8: 17,413,027-17,413,027 SLC7A2
    nsv5333289translocation1nstd200human GRCh37 chr8: 17,413,866-17,413,866 , GRCh37 chr8: 17,413,027-17,413,027 , GRCh38.p12 chr8: 17,556,357-17,556,357 , GRCh38.p12 chr8: 17,555,518-17,555,518 SLC7A2
    nsv5316314copy number variation1nstd204human GRCh38.p13 chr8: 17,555,515-17,556,366 , GRCh37.p13 chr8: 17,413,024-17,413,875 SLC7A2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5110530mobile element insertion1nstd203human GRCh38 chr8: 17,545,437-17,545,479 , GRCh37.p13 chr8: 17,402,946-17,402,988 SLC7A2
    nsv4959423copy number variation1nstd200human GRCh38 chr8: 17,497,803-17,502,479 , GRCh37.p13 chr8: 17,355,312-17,359,988 SLC7A2
    nsv4959421copy number variation1nstd200human GRCh38 chr8: 17,488,004-17,493,443 , GRCh37.p13 chr8: 17,345,513-17,350,952 SLC7A2
    nsv4959416copy number variation1nstd200human GRCh38 chr8: 17,418,992-17,544,110 , GRCh37.p13 chr8: 17,276,501-17,401,619 ADAM24P, SLC7A2
    nsv4959415copy number variation1nstd200human GRCh38 chr8: 17,418,803-17,495,613 , GRCh37.p13 chr8: 17,276,312-17,353,122 SLC7A2, ADAM24P
    nsv4954206copy number variation1nstd200human GRCh38 chr8: 17,530,701-17,861,635 , GRCh37.p13 chr8: 17,388,210-17,719,144 MTUS1, RNA5SP256, 5 more genes
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