| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | TRIM22, TRIM5 (R438C +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TRIM5, TRIM6 (H164R +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (Q221R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Copy number gain | See cases | |
| | TRIM5, TRIM6 (E183D +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (F261S +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C11orf42, MRGPRG +210 more | Copy number gain | Russell-Silver syndrome | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (R485H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (R71Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (P299T +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (C95S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (Q141R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (L139P +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | TRIM6, TRIM5 (N448T +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | TRIM6, TRIM5 (S159P +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (V134I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (H133R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIM5, TRIM6 (R256H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | TRIM6, TRIM5 (W367C +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | TRIM6, TRIM5 (R512C +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (R71W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number loss | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | TRIM5, TRIM6 (E142D +1 more) | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | AAMDC, AASDHPPT +1289 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130005185, TRIM34 +1 more (S353N) | Single nucleotide variant (missense variant +1 more) | Malignant tumor of prostate | |
| | LOC130005128, LOC130005129 +723 more | Copy number gain | See cases | |
| | A-GAMMA3'E, ABCC8 +917 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |