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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112745copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,812,675-176,813,587 , GRCh38.p12 chr5: 177,385,674-177,386,586 SLC34A1
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5962928insertion1nstd209human GRCh38 chr8: 42,533,654-42,533,654 , GRCh37.p13 chr8: 42,388,797-42,388,797 SLC20A2
    nsv5962758insertion1nstd209human GRCh38 chr8: 42,464,092-42,464,092 , GRCh37.p13 chr8: 42,321,610-42,321,610 SLC20A2
    nsv5925342copy number variation1nstd209human GRCh38 chr8: 42,482,338-42,482,429 , GRCh37.p13 chr8: 42,339,856-42,339,947 SLC20A2
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5915366copy number variation1nstd209human GRCh38 chr8: 42,441,416-42,442,062 , GRCh37.p13 chr8: 42,298,934-42,299,580 SLC20A2
    nsv5913253copy number variation1nstd209human GRCh38 chr8: 42,483,000-42,483,324 , GRCh37.p13 chr8: 42,340,518-42,340,842 SLC20A2
    nsv5911016copy number variation1nstd209human GRCh38 chr8: 42,520,414-42,522,788 , GRCh37.p13 chr: NaN-NaN SLC20A2
    nsv5906067copy number variation1nstd209human GRCh38 chr4: 22,920,705-27,042,181 , GRCh37.p13 chr4: 22,922,328-27,043,803 , SEPSECS, 49 more genes
    nsv5905899copy number variation1nstd209human GRCh38 chr5: 177,394,510-177,394,651 , GRCh37.p13 chr5: 176,821,511-176,821,652 SLC34A1
    nsv5899050copy number variation1nstd209human GRCh38 chr2: 112,543,345-112,673,811 , GRCh37.p13 chr2: 113,300,922-113,431,388 SLC20A1, POLR1B, 6 more genes
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5858923copy number variation1nstd209human GRCh38 chr8: 42,520,471-42,522,570 , GRCh37.p13 chr: NaN-NaN SLC20A2
    nsv5720218mobile element insertion1nstd211human GRCh38 chr8: 42,530,428-42,530,428 , GRCh37.p13 chr8: 42,385,571-42,385,571 SLC20A2
    nsv5704854mobile element insertion1nstd211human GRCh38 chr8: 42,438,089-42,438,089 , GRCh37.p13 chr8: 42,295,607-42,295,607 SLC20A2
    nsv5703238mobile element insertion1nstd211human GRCh38 chr8: 42,471,945-42,471,945 , GRCh37.p13 chr8: 42,329,463-42,329,463 SLC20A2
    nsv5674068copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 140,127,661-140,130,868 , GRCh38.p12 chr9: 137,233,209-137,236,416 SLC34A3
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