| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130059883, LOC130059884 +922 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | Chromosome 17p13.3 duplication syndrome | |
| | LOC121848004, LOC121848005 +457 more | Copy number loss | See cases | |
| | LOC130059937, LOC130059938 +604 more | Copy number gain | See cases | |
| | LOC130059930, LOC130059931 +352 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ALOX15, LOC126862468 (D225N) | Single nucleotide variant (missense variant) | not specified | |
| | ALOX15, LOC126862468 (R205Q) | Single nucleotide variant (missense variant) | not provided | |
| | ALOX15, LOC126862468 (W197R) | Single nucleotide variant (missense variant) | not specified | |
| | ALOX15, LOC126862468 (R165Q) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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