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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
    nsv6122723copy number variation1nstd186human GRCh37 chr13: 30,844,166-30,844,391 , GRCh38.p12 chr13: 30,270,029-30,270,254 KATNAL1
    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
    nsv5980188insertion1nstd209human GRCh38 chr13: 30,274,908-30,274,908 , GRCh37.p13 chr13: 30,849,045-30,849,045 KATNAL1
    nsv5969263insertion1nstd209human GRCh38 chr13: 30,300,907-30,300,907 , GRCh37.p13 chr13: 30,875,044-30,875,044 KATNAL1
    nsv5947441copy number variation1nstd209human GRCh38 chr13: 30,205,601-30,205,930 , GRCh37.p13 chr13: 30,779,738-30,780,067 KATNAL1
    nsv5945112copy number variation1nstd209human GRCh38 chr13: 30,269,612-30,269,847 , GRCh37.p13 chr13: 30,843,749-30,843,984 KATNAL1
    nsv5938948copy number variation1nstd209human GRCh38 chr13: 30,222,903-30,223,247 , GRCh37.p13 chr13: 30,797,040-30,797,384 KATNAL1
    nsv5937694copy number variation1nstd209human GRCh38 chr13: 30,205,606-30,205,751 , GRCh37.p13 chr13: 30,779,743-30,779,888 KATNAL1
    nsv5708242mobile element insertion1nstd211human GRCh38 chr13: 30,270,517-30,270,517 , GRCh37.p13 chr13: 30,844,654-30,844,654 KATNAL1
    nsv5655765insertion1nstd207human GRCh38 chr13: 30,271,072-30,271,072 , GRCh37.p13 chr13: 30,845,209-30,845,209 KATNAL1
    nsv5646931insertion1nstd207human GRCh38 chr13: 30,270,503-30,270,503 , GRCh37.p13 chr13: 30,844,640-30,844,640 KATNAL1
    nsv5588603copy number variation1nstd207human GRCh38 chr13: 30,270,029-30,270,253 , GRCh37.p13 chr13: 30,844,166-30,844,390 KATNAL1
    nsv5587800copy number variation1nstd207human GRCh38 chr13: 30,236,274-30,239,432 , GRCh37.p13 chr13: 30,810,411-30,813,569 LOC102723381, KATNAL1
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5513191copy number variation1nstd206human GRCh38 chr13: 30,009,700-30,223,000 , GRCh37.p13 chr13: 30,583,837-30,797,137 LINC00365, LINC00384, 2 more genes
    nsv5505705copy number variation1nstd206human GRCh38 chr13: 30,270,029-30,270,254 , GRCh37.p13 chr13: 30,844,166-30,844,391 KATNAL1
    nsv5504885copy number variation1nstd206human GRCh38 chr13: 30,251,052-30,253,621 , GRCh37.p13 chr13: 30,825,189-30,827,758 KATNAL1
    nsv5494560copy number variation1nstd206human GRCh38 chr13: 30,207,530-30,210,476 , GRCh37.p13 chr13: 30,781,667-30,784,613 KATNAL1
    nsv5427100mobile element insertion1nstd206human GRCh38 chr13: 30,270,517-30,270,568 , GRCh37.p13 chr13: 30,844,654-30,844,705 KATNAL1
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