| | LCA5L, LINC00111 +1159 more | Copy number gain | See cases | |
| | LOC126653353, LOC126653354 +1160 more | Copy number gain | See cases | |
| | KRTAP8-1, LCA5L +1160 more | Copy number gain | See cases | |
| | RNA5-8SN1, RNA5-8SN2 +1160 more | Copy number gain | See cases | |
| | LOC130066804, LOC130066805 +1160 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126653353, LOC126653354 +1159 more | Copy number gain | See cases | |
| | LOC129388418, LOC129391214 +1160 more | Copy number gain | See cases | |
| | KCNJ6, KCNJ6-AS1 +643 more | 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 | |
| | LINC00515, LINC00649 +1159 more | Copy number gain | See cases | |
| | LOC130066731, LOC130066732 +1159 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ETS2-AS1, EVA1C +1157 more | Copy number gain | See cases | |
| | LOC130066726, LOC130066727 +1159 more | Copy number gain | See cases | |
| | LOC128849172, LOC129388418 +884 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC01425, LINC01426 +1157 more | Copy number gain | See cases | |
| | LOC130066861, LOC130066862 +1155 more | Copy number gain | See cases | |
| | LOC130066468, LOC130066469 +1155 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC112694754, LOC114004360 +1159 more | Copy number gain | See cases | |
| | LOC130066795, LOC130066796 +1156 more | Copy number loss | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | LOC130066604, LOC130066605 +23 more | Deletion | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Deletion (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Microsatellite (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Microsatellite (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Duplication (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Duplication (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Duplication (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Deletion (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | LINC01424, LINC01436 +643 more | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Deletion (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |