| | LOC129931453, LOC129931454 +1585 more | Copy number gain | See cases | |
| | | Single nucleotide variant | Kostmann syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Deletion (5 prime UTR variant) | Severe congenital neutropenia | |
| | | Deletion (5 prime UTR variant) | not provided | |
| | | Indel (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | Kostmann syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Deletion (nonsense) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome +1 more | |
| | | Deletion (frameshift variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kostmann syndrome | |
| | | Single nucleotide variant (nonsense) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome | |
| | | Microsatellite (intron variant) | Kostmann syndrome | |
| | | Insertion (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Deletion (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (intron variant) | Kostmann syndrome | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Kostmann syndrome | |
| | | Duplication (frameshift variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Indel (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Kostmann syndrome | |
| | | Microsatellite (inframe_indel +2 more) | HAX1-related disorder | |
| | | Deletion (inframe_deletion +1 more) | Kostmann syndrome | |
| | | Deletion (frameshift variant +1 more) | Severe congenital neutropenia +2 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Duplication (inframe_insertion +1 more) | Kostmann syndrome | |
| | | Deletion (frameshift variant +1 more) | Kostmann syndrome | |
| | | Deletion (inframe_deletion +1 more) | Kostmann syndrome | |
| | | Microsatellite (inframe_insertion +1 more) | Kostmann syndrome | |
| | | Microsatellite (inframe_insertion +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Microsatellite (inframe_deletion +1 more) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | HAX1-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Duplication (inframe_insertion +1 more) | Kostmann syndrome +1 more | |
| | | Duplication (frameshift variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Insertion (nonsense +1 more) | not provided +1 more | |
| | | Deletion (inframe_deletion +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Deletion (frameshift variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome +1 more | |
| | | Duplication (intron variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Kostmann syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Kostmann syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Kostmann syndrome | |
| | | Deletion (frameshift variant +1 more) | Kostmann syndrome | |
| | | Duplication (frameshift variant +1 more) | Kostmann syndrome | |
| | | Deletion (intron variant +1 more) | Kostmann syndrome | |