| | LOC129931453, LOC129931454 +1585 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ADAMTS4, ALDH9A1 +371 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Developmental and epileptic encephalopathy 98 +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (splice donor variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (splice donor variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Deletion (intron variant) | Familial hemiplegic migraine | |
| | | 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) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Deletion (intron variant) | not provided | |
| | | Deletion (intron variant) | not specified | |
| | | Deletion (intron variant) | Alternating hemiplegia of childhood +6 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +3 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine +2 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Alternating hemiplegia of childhood 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine | |