| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant | not specified +1 more | |
| | | Single nucleotide variant | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Isovaleryl-CoA dehydrogenase deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Isovaleryl-CoA dehydrogenase deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +3 more) | not provided | |
| | | Single nucleotide variant (missense variant +3 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency +2 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Deletion (nonsense +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Deletion (frameshift variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Deletion (frameshift variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | |
| | | Duplication (frameshift variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleric acidemia, type I | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Deletion (5 prime UTR variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Microsatellite (5 prime UTR variant +2 more) | not provided | |
| | | Microsatellite (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Isovaleryl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | GPathogenic/Likely pathogenic |