| | | Copy number gain | See cases | |
| | LOC129935343, LOC129935344 +1687 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129935480, LOC129935481 +1299 more | Copy number gain | See cases | |
| | LOC129935841, LOC129935842 +1148 more | Copy number gain | See cases | |
| | LOC129935871, LOC129935872 +986 more | Copy number gain | See cases | |
| | LOC126806566, LOC126806567 +393 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129935973, LOC129935974 +576 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129935973, LOC129935974 +455 more | Copy number loss | See cases | |
| | LOC129935990, LOC129935991 +361 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | 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 (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | UGT1A, UGT1A10 +1 more (V10I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (P11A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (L18P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (G21A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (G26E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (H53L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (L117P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (C124R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (G196R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +1 more (V212L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (H217N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (A231T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (P238L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (Y261C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (V265M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +1 more (C277R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | UGT1A, UGT1A10 +2 more (E24K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A9, UGT1A +2 more (M33T) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +2 more (D34G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (S43L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (V62A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | UGT1A9-related disorder | |
| | UGT1A, UGT1A10 +2 more (T73A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (K75R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +1 more | |
| | UGT1A, UGT1A10 +2 more (S126N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (L133I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | UGT1A9-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | UGT1A9-related disorder | |
| | UGT1A, UGT1A10 +2 more (D143E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | UGT1A9-related disorder | |
| | UGT1A, UGT1A10 +2 more (L155V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (V167A) | Single nucleotide variant (missense variant +1 more) | UGT1A9-related disorder | |
| | UGT1A, UGT1A10 +2 more (G171V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (H175R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (A185T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (R206G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (H221R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (A227V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (T255M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (F257V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +2 more (V258A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +3 more (A23D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (G35E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A8, UGT1A7 +3 more (M41I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (V58F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (W64*) | Single nucleotide variant (nonsense +1 more) | not provided | |
| | UGT1A, UGT1A10 +3 more (Y81*) | Single nucleotide variant (nonsense +1 more) | not provided | |
| | UGT1A9, UGT1A8 +3 more (R88W) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | UGT1A8, UGT1A10 +3 more (F90L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (V92I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (D95N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | UGT1A, UGT1A10 +3 more (N114S) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +3 more (G115S) | Single nucleotide variant (intron variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +3 more (D118Y) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +3 more (S122P) | Single nucleotide variant (missense variant +1 more) | not specified | |