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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072946inversion1nstd229human GRCh38 chr13: 28,026,508-28,026,541 , GRCh37.p13 chr13: 28,600,645-28,600,678 FLT3
    nsv7069896inversion1nstd229human GRCh38 chr13: 28,062,232-28,062,342 , GRCh37.p13 chr13: 28,636,369-28,636,479 FLT3
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6936740copy number variation1nstd229human GRCh38 chr13: 28,089,367-28,090,338 , GRCh37.p13 chr13: 28,663,504-28,664,475 FLT3
    nsv6936652copy number variation1nstd229human GRCh38 chr13: 28,011,301-28,018,100 , GRCh37.p13 chr13: 28,585,438-28,592,237 FLT3
    nsv6936051copy number variation1nstd229human GRCh38 chr13: 28,080,601-28,100,200 , GRCh37.p13 chr13: 28,654,738-28,674,337 FLT3
    nsv6934224copy number variation1nstd229human GRCh38 chr13: 28,079,949-28,086,743 , GRCh37.p13 chr13: 28,654,086-28,660,880 FLT3
    nsv6933198copy number variation1nstd229human GRCh38 chr13: 28,085,401-28,125,300 , GRCh37.p13 chr13: 28,659,538-28,699,437 FLT3, CHCHD2P8
    nsv6932205copy number variation1nstd229human GRCh38 chr13: 27,994,607-28,002,806 , GRCh37.p13 chr13: 28,568,744-28,576,943 FLT3
    nsv6932013copy number variation1nstd229human GRCh38 chr13: 27,894,801-28,169,500 , GRCh37.p13 chr13: 28,468,938-28,743,637 URAD, CDX2, 12 more genes
    nsv6931589copy number variation1nstd229human GRCh38 chr13: 28,049,901-28,107,900 , GRCh37.p13 chr13: 28,624,038-28,682,037 CHCHD2P8, KATNBL1P1, 1 more genes
    nsv6930748copy number variation1nstd229human GRCh38 chr13: 28,051,805-28,052,356 , GRCh37.p13 chr13: 28,625,942-28,626,493 FLT3
    nsv6930602copy number variation1nstd229human GRCh38 chr13: 28,034,557-28,034,718 , GRCh37.p13 chr13: 28,608,694-28,608,855 FLT3
    nsv6930050copy number variation1nstd229human GRCh38 chr13: 28,086,016-28,096,578 , GRCh37.p13 chr13: 28,660,153-28,670,715 FLT3
    nsv6928030copy number variation1nstd229human GRCh38 chr13: 28,040,349-28,043,139 , GRCh37.p13 chr13: 28,614,486-28,617,276 FLT3
    nsv6923079copy number variation1nstd229human GRCh38 chr13: 28,065,671-28,065,858 , GRCh37.p13 chr13: 28,639,808-28,639,995 KATNBL1P1, FLT3
    nsv6922729copy number variation1nstd229human GRCh38 chr13: 27,992,817-28,016,865 , GRCh37.p13 chr13: 28,566,954-28,591,002 FLT3
    nsv6921864copy number variation1nstd229human GRCh38 chr13: 28,009,953-28,013,695 , GRCh37.p13 chr13: 28,584,090-28,587,832 FLT3
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6593485inversion1nstd223human GRCh38 chr13: 28,039,837-28,040,506 , GRCh37.p13 chr13: 28,613,974-28,614,643 FLT3
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