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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5974110inversion1nstd209human GRCh37.p13 chr5: 40,662,872-40,710,021 , GRCh38 chr5: 40,662,770-40,709,919 PTGER4, TTC33
    nsv5890336copy number variation1nstd209human GRCh38 chr5: 40,694,448-40,694,561 , GRCh37.p13 chr5: 40,694,550-40,694,663 PTGER4
    nsv5843043copy number variation1nstd209human GRCh38 chr5: 40,714,090-40,715,489 , GRCh37.p13 chr5: 40,714,192-40,715,591 PTGER4, TTC33
    nsv5634255insertion1nstd207human GRCh38 chr5: 40,694,448-40,694,448 , GRCh37.p13 chr5: 40,694,550-40,694,550 PTGER4
    nsv5580673copy number variation1nstd207human GRCh38 chr5: 40,735,763-40,740,479 , GRCh37.p13 chr5: 40,735,865-40,740,581 PTGER4, TTC33
    nsv5578694copy number variation1nstd207human GRCh38 chr5: 40,697,060-40,697,115 , GRCh37.p13 chr5: 40,697,162-40,697,217 PTGER4
    nsv5559749sequence alteration1nstd206human GRCh38 chr5: 40,738,885-40,738,899 , GRCh37.p13 chr5: 40,738,987-40,739,001 PTGER4, TTC33
    nsv5546256insertion1nstd206human GRCh38 chr5: 40,738,885-40,738,885 , GRCh37.p13 chr5: 40,738,987-40,738,987 PTGER4, TTC33
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5466387copy number variation1nstd206human GRCh38 chr5: 40,694,448-40,694,562 , GRCh37.p13 chr5: 40,694,550-40,694,664 PTGER4
    nsv5458256copy number variation1nstd206human GRCh38 chr5: 40,707,671-40,708,290 , GRCh37.p13 chr5: 40,707,773-40,708,392 PTGER4
    nsv5456634copy number variation1nstd206human GRCh38 chr5: 40,735,766-40,740,480 , GRCh37.p13 chr5: 40,735,868-40,740,582 PTGER4, TTC33
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368207translocation1nstd200human GRCh38 chr22: 28,669,391-28,669,391 , GRCh38 chr5: 40,729,104-40,729,104 , GRCh37.p13 chr22: 29,065,379-29,065,379 , GRCh37.p13 chr5: 40,729,206-40,729,206 PTGER4, TTC28, 1 more genes
    nsv5185437mobile element insertion1nstd203human GRCh38 chr5: 40,735,589-40,735,589 , GRCh37.p13 chr5: 40,735,691-40,735,691 PTGER4, TTC33
    nsv5099611mobile element insertion1nstd203human GRCh38 chr5: 40,738,472-40,738,516 , GRCh37.p13 chr5: 40,738,574-40,738,618 PTGER4, TTC33
    nsv5097904mobile element insertion1nstd203human GRCh38 chr5: 40,738,482-40,738,518 , GRCh37.p13 chr5: 40,738,584-40,738,620 PTGER4, TTC33
    nsv5095421mobile element insertion1nstd203human GRCh38 chr5: 40,738,507-40,738,518 , GRCh37.p13 chr5: 40,738,609-40,738,620 PTGER4, TTC33
    nsv5094395mobile element insertion1nstd203human GRCh38 chr5: 40,715,401-40,715,414 , GRCh37.p13 chr5: 40,715,503-40,715,516 PTGER4, TTC33
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