| | | Single nucleotide variant (synonymous variant +3 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | FCGR1A, H2BC18 (Q41E +3 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (R92* +3 more) | Single nucleotide variant (intron variant +2 more) | IGG receptor I, phagocytic, familial deficiency of | |
| | FCGR1A, H2BC18 (R176C +5 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (Q139K +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (Q246* +6 more) | Single nucleotide variant (nonsense +2 more) | Peritoneal Gliomatosis | |
| | FCGR1A, H2BC18 (R188C +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (E193Q +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (E192D +6 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (M193T +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (M218I +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (T203K +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (R205C +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (I229T +8 more) | Single nucleotide variant (missense variant +2 more) | not provided | |
| | FCGR1A, H2BC18 (L318F +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (E359del +8 more) | Microsatellite (inframe_indel +3 more) | not provided | |
| | FCGR1A, H2BC18 (G272V +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (V273L +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | FCGR1A, H2BC18 (E346Q +8 more) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | | Copy number gain | See cases | |
| | | Copy number loss | not provided | |
| | | Duplication | Parathyroid carcinoma +2 more | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |