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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097257copy number variation1nstd102humanPathogenic GRCh37 chr4: 55,569,880-55,570,068 , GRCh38.p12 chr4: 54,703,714-54,703,902 KIT
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7097000copy number variation1nstd102humanUncertain significance GRCh37 chr4: 55,604,585-55,604,723 , GRCh38.p12 chr4: 54,738,419-54,738,557 KIT
    nsv7096862copy number variation1nstd102humanUncertain significance GRCh37 chr4: 55,589,740-55,604,723 , GRCh38.p12 chr4: 54,723,574-54,738,557 KIT
    nsv7096861copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 55,575,570-55,598,184 , GRCh38.p12 chr4: 54,709,404-54,732,018 KIT
    nsv7053546inversion1nstd229human GRCh38 chr4: 54,555,777-54,810,710 , GRCh37.p13 chr4: 55,421,944-55,676,876 KIT, LINC02260, 1 more genes
    nsv6733756copy number variation1nstd229human GRCh38 chr4: 54,690,423-54,690,818 , GRCh37.p13 chr4: 55,556,589-55,556,984 KIT
    nsv6733345copy number variation1nstd229human GRCh38 chr4: 54,674,300-54,684,412 , GRCh37.p13 chr4: 55,540,466-55,550,578 KIT
    nsv6733289copy number variation1nstd229human GRCh38 chr4: 54,664,552-54,664,646 , GRCh37.p13 chr4: 55,530,718-55,530,812 KIT
    nsv6731518copy number variation1nstd229human GRCh38 chr4: 54,667,718-54,667,744 , GRCh37.p13 chr4: 55,533,884-55,533,910 KIT
    nsv6730119copy number variation1nstd229human GRCh38 chr4: 54,711,649-54,711,726 , GRCh37.p13 chr4: 55,577,815-55,577,892 KIT
    nsv6727319copy number variation1nstd229human GRCh38 chr4: 54,703,301-54,707,200 , GRCh37.p13 chr4: 55,569,467-55,573,366 KIT
    nsv6726521copy number variation1nstd229human GRCh38 chr4: 54,659,197-54,667,504 , GRCh37.p13 chr4: 55,525,364-55,533,670 KIT
    nsv6726290copy number variation1nstd229human GRCh38 chr4: 54,301,171-54,691,127 , GRCh37.p13 chr4: 55,167,338-55,557,293 LINC02260, KIT, 1 more genes
    nsv6720227copy number variation1nstd229human GRCh38 chr4: 54,720,704-54,721,288 , GRCh37.p13 chr4: 55,586,870-55,587,454 KIT
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6636076copy number variation1nstd102humanUncertain significance GRCh38 chr4: 54,711,645-54,711,721 , GRCh37 chr4: 55,577,811-55,577,887 KIT
    nsv6567636inversion1nstd223human GRCh38 chr4: 54,555,777-54,810,711 , GRCh37.p13 chr4: 55,421,944-55,676,877 KIT, LINC02260, 1 more genes
    nsv6395210copy number variation1nstd223human GRCh38 chr4: 54,688,399-54,688,788 , GRCh37.p13 chr4: 55,554,565-55,554,954 KIT
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