| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Insertion (intron variant) | Human immunodeficiency virus type 1, rapid progression to AIDS | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | not provided | |
| | | 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 | |
| | LOC130064107, LOC130064108 +574 more | Copy number gain | See cases | |
| | LOC130064390, LOC130064391 +2135 more | Copy number gain | See cases | |
| | LOC130063908, LOC130063909 +695 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
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