| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129936144, LOC129936145 +271 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC112935932, LOC112935963 +331 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936094, LOC129936095 +647 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936377, LOC129936378 +1111 more | Copy number gain | See cases | |
| | LOC110120630, LOC111429626 +608 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +307 more | Copy number gain | See cases | |
| | LOC129929025, LOC129929026 +190 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +146 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +81 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +118 more | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +63 more | Copy number loss | See cases | |
| | LOC129936140, LOC129936141 +58 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Chuvash polycythemia +1 more | |
| | | Duplication | Chuvash polycythemia +1 more | |
| | | Duplication | Chuvash polycythemia +1 more | |
| | | Deletion | Fanconi anemia | |
| | LOC107303340, LOC129936148 +7 more | Deletion | Von Hippel-Lindau syndrome +1 more | |
| | | Deletion | Pancreatic cysts +1 more | |
| | LOC107303339, LOC107303340 +1 more | Deletion | Von Hippel-Lindau syndrome | |
| | LOC107303339, LOC107303340 +1 more | Deletion | Von Hippel-Lindau syndrome | |
| | LOC107303340, LOC107303339 +1 more | Deletion | Von Hippel-Lindau syndrome | |
| | LOC107303340, LOC107303339 +1 more | Deletion | Von Hippel-Lindau syndrome | |
| | LOC107303339, LOC107303340 +1 more | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Insertion | not provided | |
| | | Duplication | not provided | |
| | | Duplication | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | Von Hippel-Lindau syndrome +1 more | |
| | | Deletion | Von Hippel-Lindau syndrome +1 more | |
| | | Single nucleotide variant | Chuvash polycythemia +3 more | |
| | | Single nucleotide variant | Chuvash polycythemia +2 more | |
| | | Single nucleotide variant | not specified +1 more | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | not specified | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | not specified | |
| | | Single nucleotide variant | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Deletion | Chuvash polycythemia | |
| | | Deletion | Chuvash polycythemia +1 more | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Deletion | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome +2 more | |
| | | Single nucleotide variant | Von Hippel-Lindau syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Duplication (5 prime UTR variant) | VHL-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | VHL-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (5 prime UTR variant +1 more) | not provided | |
| | | Duplication (5 prime UTR variant) | VHL-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (5 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Chuvash polycythemia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Chuvash polycythemia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Chuvash polycythemia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | Chuvash polycythemia +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Von Hippel-Lindau syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (5 prime UTR variant +1 more) | Chuvash polycythemia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Chuvash polycythemia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | VHL-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | VHL-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | Von Hippel-Lindau syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Duplication (inframe_insertion +2 more) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Indel (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Duplication (frameshift variant +1 more) | VHL-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Deletion | Chuvash polycythemia +1 more | |