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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5979785insertion1nstd209human GRCh38 chr13: 29,555,357-29,555,357 , GRCh37.p13 chr13: 30,129,494-30,129,494 SLC7A1
    nsv5725522mobile element insertion1nstd211human GRCh38 chr13: 29,540,503-29,540,503 , GRCh37.p13 chr13: 30,114,640-30,114,640 SLC7A1
    nsv5716194mobile element insertion1nstd211human GRCh38 chr13: 29,575,779-29,575,779 , GRCh37.p13 chr13: 30,149,916-30,149,916 SLC7A1
    nsv5662854insertion1nstd207human GRCh38 chr13: 29,555,357-29,555,357 , GRCh37.p13 chr13: 30,129,494-30,129,494 SLC7A1
    nsv5660350insertion1nstd207human GRCh38 chr13: 29,558,730-29,558,730 , GRCh37.p13 chr13: 30,132,867-30,132,867 SLC7A1
    nsv5659683insertion1nstd207human GRCh38 chr13: 29,559,150-29,559,150 , GRCh37.p13 chr13: 30,133,287-30,133,287 SLC7A1
    nsv5655021insertion1nstd207human GRCh38 chr13: 29,558,208-29,558,208 , GRCh37.p13 chr13: 30,132,345-30,132,345 SLC7A1
    nsv5653641insertion1nstd207human GRCh38 chr13: 29,558,500-29,558,500 , GRCh37.p13 chr13: 30,132,637-30,132,637 SLC7A1
    nsv5650813insertion1nstd207human GRCh38 chr13: 29,559,411-29,559,411 , GRCh37.p13 chr13: 30,133,548-30,133,548 SLC7A1
    nsv5650398insertion1nstd207human GRCh38 chr13: 29,558,269-29,558,269 , GRCh37.p13 chr13: 30,132,406-30,132,406 SLC7A1
    nsv5647550insertion1nstd207human GRCh38 chr13: 29,559,049-29,559,049 , GRCh37.p13 chr13: 30,133,186-30,133,186 SLC7A1
    nsv5645086insertion1nstd207human GRCh38 chr13: 29,557,833-29,557,833 , GRCh37.p13 chr13: 30,131,970-30,131,970 SLC7A1
    nsv5602418copy number variation1nstd207human GRCh38 chr13: 29,557,969-29,558,528 , GRCh37.p13 chr13: 30,132,106-30,132,665 SLC7A1
    nsv5602160copy number variation1nstd207human GRCh38 chr13: 29,559,001-29,559,064 , GRCh37.p13 chr13: 30,133,138-30,133,201 SLC7A1
    nsv5601773copy number variation1nstd207human GRCh38 chr13: 29,558,652-29,558,729 , GRCh37.p13 chr13: 30,132,789-30,132,866 SLC7A1
    nsv5601446copy number variation1nstd207human GRCh38 chr13: 29,558,980-29,559,258 , GRCh37.p13 chr13: 30,133,117-30,133,395 SLC7A1
    nsv5598021copy number variation1nstd207human GRCh38 chr13: 29,559,453-29,559,512 , GRCh37.p13 chr13: 30,133,590-30,133,649 SLC7A1
    nsv5594332copy number variation1nstd207human GRCh38 chr13: 29,558,512-29,558,569 , GRCh37.p13 chr13: 30,132,649-30,132,706 SLC7A1
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