| | LOC130001537, LOC130001538 +3785 more | Copy number gain | See cases | |
| | LOC130002976, LOC130002977 +3784 more | Copy number gain | See cases | |
| | LOC130001468, LOC130001469 +3785 more | Copy number gain | See cases | |
| | DNAJB5, DNAJB5-DT +3785 more | Copy number gain | See cases | |
| | LOC114827838, LOC116186936 +3785 more | Copy number gain | See cases | |
| | LOC124252641, LOC124252642 +3785 more | Copy number gain | See cases | |
| | LOC114022701, LOC114022702 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC110120726, LOC110120727 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130002218, LOC130002219 +994 more | Copy number gain | See cases | |
| | LOC130002205, LOC130002206 +417 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126860732, LOC126860733 +514 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Weiss-kruszka syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC130002268, NIPSNAP3B (L12F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Duplication (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Tangier disease +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypoalphalipoproteinemia, primary, 1 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial High Density Lipoprotein Deficiency +1 more | |