| | LOC130004500, LOC130004501 +821 more | Copy number gain | See cases | |
| | EDRF1-AS1, EDRF1-DT +1036 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Desmoplastic/nodular medulloblastoma | |
| | | Copy number loss | See cases | |
| | LOC124416905, LOC124416906 +318 more | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary spastic paraplegia +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | CNNM2, LOC130004629 +1 more | Deletion | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Microsatellite (inframe_insertion +1 more) | Hereditary spastic paraplegia 45 | |
| | | Microsatellite (inframe_insertion +1 more) | Hereditary spastic paraplegia 45 | |
| | | Microsatellite (inframe_insertion +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (E323del +5 more) | Microsatellite (inframe_deletion +1 more) | Hereditary spastic paraplegia 45 +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion +1 more) | Hereditary spastic paraplegia 45 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Deletion (inframe_deletion +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (E555D +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (E370del +5 more) | Deletion (inframe_deletion +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (Q304fs +5 more) | Deletion (frameshift variant +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (A302V +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 45 | |
| | NT5C2, CNNM2 (A509T +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (I500V +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CNNM2, NT5C2 (I499V +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | NT5C2, CNNM2 (H284Y +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | CNNM2, NT5C2 (R283Q +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia | |
| | CNNM2, NT5C2 (K329R +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | NT5C2-related disorder | |
| | NT5C2, CNNM2 (T272I +5 more) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 45 | |
| | CNNM2, NT5C2 (T479P +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | CNNM2, NT5C2 (D305H +5 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (splice donor variant) | Neurodevelopmental disorder +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 +1 more | |
| | | Duplication (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Deletion (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Deletion (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Deletion (frameshift variant) | Hereditary spastic paraplegia 45 | |
| | | Duplication (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Deletion (intron variant) | NT5C2-related disorder +1 more | |
| | | Deletion (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Duplication (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (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) | Hereditary spastic paraplegia 45 +1 more | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (splice donor variant) | Hereditary spastic paraplegia 45 | |
| | | Deletion (frameshift variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 45 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 45 | |