| | | Copy number gain | See cases | |
| | LOC129999937, LOC129999938 +3658 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126860501, LOC126860502 +3652 more | Copy number gain | See cases | |
| | MIR7705, MIR7848 +3656 more | Copy number gain | See cases | |
| | LOC130000156, LOC130000157 +3106 more | Copy number gain | See cases | |
| | LINC02894, LINC02906 +1960 more | Copy number gain | See cases | |
| | LOC130000438, LOC130000439 +421 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130000602, LOC130000603 +470 more | Copy number gain | See cases | |
| | LOC130000640, LOC130000641 +245 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Charcot-Marie-Tooth disease axonal type 2K | |
| | LOC130000617, LOC130000618 +191 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Microsatellite | not provided | |
| | | Microsatellite | not provided | |
| | | Microsatellite | not provided | |
| | | Microsatellite | not provided | |
| | | Microsatellite | not provided | |
| | | Single nucleotide variant | Mitochondrial proton-transporting ATP synthase complex deficiency | |
| | | Duplication (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 +1 more | |
| | | Duplication | Charcot-Marie-Tooth disease type 4A | |
| | | Deletion | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Indel (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Duplication (frameshift variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Microsatellite (inframe_deletion +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Duplication (inframe_insertion +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Duplication (frameshift variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | TMEM70-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Duplication (frameshift variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 +1 more | |
| | | Duplication (frameshift variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Deletion (inframe_deletion +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Deletion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Duplication (frameshift variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | |