| | | Copy number loss | Chromosome 4q21 deletion syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129993082, LOC129993083 +661 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ADH4, LOC100507053 (R375Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (F358S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (L367V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (R318L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (R318C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (I298T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (F235L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (N231S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (A241T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (L230P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (V209L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (C201Y +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (A207V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (F146L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (K151T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (I111T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (P106R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (V85I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (A72V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (H88R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (V86A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (V67I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (A62P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (K52E +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC100507053, ADH4 (P32R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (P32L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (E28K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (P21A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADH4, LOC100507053 (A18fs +1 more) | Duplication (frameshift variant) | CIC-rearranged sarcoma | |
| | ADH4, LOC100507053 (A15T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |