| | LOC130064390, LOC130064391 +2135 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130064198, LOC132090533 +210 more | Copy number gain | See cases | |
| | LOC130064186, LOC130064187 +459 more | Copy number loss | See cases | |
| | LOC130064234, LOC130064235 +439 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC130064162, NUDT19 +1 more (S3N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC130064162, NUDT19 +1 more (R6W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (A21E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (A22P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (G23D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (L44Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (L47R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (R49C) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC130064162, NUDT19 +1 more (D71N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064162, NUDT19 +1 more (R72P) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Duplication | Hereditary spastic paraplegia 75 | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | Specific learning disability | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |