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Items: 53

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANKRD28, ARL8B
+799 more
Copy number gain
See cases
GPathogenic
LOC129936198, LOC129936199
+647 more
Copy number gain
See cases
GPathogenic
LOC129936421, LOC129936422
+962 more
Copy number gain
See cases
GPathogenic
ACAA1, ACVR2B
+1111 more
Copy number gain
See cases
GPathogenic
LOC110120630, LOC111429626
+608 more
Copy number gain
See cases
GPathogenic
LOC132088948, LOC132088950
+730 more
Copy number gain
See cases
GPathogenic
HDAC11, LOC126806611
+244 more
Deletion
3p- syndrome
GPathogenic
LOC132088880, LOC132088882
+214 more
Copy number gain
See cases
GPathogenic
DAZL
(D274E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(R250Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
Single nucleotide variant
(intron variant)
DAZL-related disorder
GBenign
DAZL
(G242D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(H253R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(P241L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(H215N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(R201K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(P213S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(M191L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
Duplication
(intron variant)
DAZL-related disorder
GBenign
DAZL
Single nucleotide variant
(synonymous variant)
DAZL-related disorder
GLikely benign
DAZL
(Q183R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(V178F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(V165A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(N165K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
Single nucleotide variant
(synonymous variant)
DAZL-related disorder
GBenign
DAZL
(H133R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(N152S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(N122H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
Single nucleotide variant
(synonymous variant)
Idiopathic male infertility
Gassociation
DAZL
Single nucleotide variant
(synonymous variant)
Idiopathic male infertility
Gassociation
DAZL
(D74fs +1 more)
Duplication
(frameshift variant)
Idiopathic male infertility
GPathogenic
DAZL
(V66E +1 more)
Single nucleotide variant
(missense variant)
Idiopathic male infertility
GLikely pathogenic
DAZL
(S65T +1 more)
Single nucleotide variant
(missense variant)
Idiopathic male infertility
GBenign
DAZL
(R82K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(E55D +1 more)
Single nucleotide variant
(missense variant)
Idiopathic male infertility
GBenign
DAZL
(T54A +1 more)
Single nucleotide variant
(missense variant)
Spermatogenic failure, susceptibility to
Grisk factor
DAZL
(T12A +1 more)
Single nucleotide variant
(missense variant)
DAZL-related disorder
GBenign
DAZL
(N5S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DAZL
(T3A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DAZL
(C6Y)
Single nucleotide variant
(missense variant +1 more)
DAZL-related disorder
GBenign
ANKRD28, ARL8B
+145 more
Copy number gain
not provided
GPathogenic
OXTR, PDCD6IP
+145 more
Copy number gain
not specified
GPathogenic
ANKRD28, ARL8B
+121 more
Copy number gain
not provided
GPathogenic
ANKRD28, BTD
+41 more
Copy number gain
See cases
GPathogenic
FANCD2OS, THUMPD3
+148 more
Copy number gain
not specified
GPathogenic
ANKRD28, ARL8B
+112 more
Copy number gain
not specified
GPathogenic
ANKRD28, ARL8B
+84 more
Copy number gain
not provided
GPathogenic
ANKRD28, ARL8B
+98 more
Copy number gain
not provided
GPathogenic
ANKRD28, BTD
+27 more
Copy number loss
See cases
GLikely pathogenic
ANKRD28, APRG1
+155 more
Copy number gain
See cases
GPathogenic
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
TRIM71, TRNT1
+145 more
Copy number gain
See cases
GPathogenic
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