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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966988insertion1nstd209human GRCh38 chr9: 128,353,758-128,353,758 , GRCh37.p13 chr9: 131,116,037-131,116,037 SLC27A4
    nsv5914432copy number variation1nstd209human GRCh38 chr9: 128,356,700-128,356,849 , GRCh37.p13 chr9: 131,118,979-131,119,128 SLC27A4
    nsv5643393insertion1nstd207human GRCh38 chr9: 128,353,758-128,353,758 , GRCh37.p13 chr9: 131,116,037-131,116,037 SLC27A4
    nsv5591005copy number variation1nstd207human GRCh38 chr9: 128,356,700-128,356,849 , GRCh37.p13 chr9: 131,118,979-131,119,128 SLC27A4
    nsv5477710copy number variation1nstd206human GRCh38 chr9: 128,356,711-128,356,818 , GRCh37.p13 chr9: 131,118,990-131,119,097 SLC27A4
    nsv5387432copy number variation2nstd186human GRCh37 chr9: 131,118,990-131,119,097 , GRCh38.p12 chr9: 128,356,711-128,356,818 SLC27A4
    nsv5373127translocation1nstd200human GRCh38 chr9: 128,340,741-128,340,741 , GRCh38 chr9: 128,340,669-128,340,669 , GRCh37.p13 chr9: 131,102,948-131,102,948 , GRCh37.p13 chr9: 131,103,020-131,103,020 SLC27A4, TMSB4XP4
    nsv5334436translocation1nstd200human GRCh37 chr9: 131,103,020-131,103,020 , GRCh37 chr9: 131,102,948-131,102,948 , GRCh38.p12 chr9: 128,340,669-128,340,669 , GRCh38.p12 chr9: 128,340,741-128,340,741 TMSB4XP4, SLC27A4
    nsv5309946copy number variation1nstd204human GRCh38.p13 chr9: 128,356,711-128,356,820 , GRCh37.p13 chr9: 131,118,990-131,119,099 SLC27A4
    nsv5132036mobile element insertion1nstd203human GRCh38 chr9: 128,353,771-128,353,820 , GRCh37.p13 chr9: 131,116,050-131,116,099 SLC27A4
    nsv5131106mobile element insertion1nstd203human GRCh38 chr9: 128,353,820-128,353,827 , GRCh37.p13 chr9: 131,116,099-131,116,106 SLC27A4
    nsv5126774mobile element insertion1nstd203human GRCh38 chr9: 128,353,802-128,353,820 , GRCh37.p13 chr9: 131,116,081-131,116,099 SLC27A4
    nsv5124228mobile element insertion1nstd203human GRCh38 chr9: 128,351,374-128,351,383 , GRCh37.p13 chr9: 131,113,653-131,113,662 SLC27A4
    nsv5121763mobile element insertion1nstd203human GRCh38 chr9: 128,353,770-128,353,820 , GRCh37.p13 chr9: 131,116,049-131,116,099 SLC27A4
    nsv4988386copy number variation1nstd200human GRCh38 chr9: 128,356,711-128,356,818 , GRCh37.p13 chr9: 131,118,990-131,119,097 SLC27A4
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4843778copy number variation1nstd200human GRCh37 chr9: 131,118,990-131,119,097 , GRCh38.p12 chr9: 128,356,711-128,356,818 SLC27A4
    nsv4841204copy number variation1nstd200human GRCh37 chr9: 131,115,636-131,116,314 , GRCh38.p12 chr9: 128,353,357-128,354,035 SLC27A4
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 COQ4, GLE1, 53 more genes
    nsv4754867insertion1nstd199human GRCh37 chr9: 131,116,034-131,116,034 , GRCh38.p12 chr9: 128,353,755-128,353,755 SLC27A4
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