| | LOC130057927, LOC130057928 +1764 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC116268473, LOC116268474 +1244 more | Copy number gain | See cases | |
| | | Duplication | Schizophrenia | |
| | LOC130057730, LOC132090332 +175 more | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple acyl-CoA dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple acyl-CoA dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Deletion (3 prime UTR variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (stop lost) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (splice acceptor variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (splice acceptor variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency +1 more | |
| | | Duplication (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (splice donor variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (inframe_deletion) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Duplication (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Insertion (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Duplication (frameshift variant) | Multiple acyl-CoA dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Multiple acyl-CoA dehydrogenase deficiency | |