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Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130060335, LOC130060336
+242 more
Copy number gain
See cases
GPathogenic
ADORA2B, ARHGAP44
+228 more
Duplication
not specified
GPathogenic
ADORA2B, CCDC144A
+137 more
Copy number loss
See cases
GPathogenic
LOC284191, LRRC75A
+216 more
Copy number gain
See cases
GPathogenic
ADORA2B, AKAP10
+333 more
Copy number gain
See cases
GPathogenic
ADORA2B, AKAP10
+337 more
Copy number gain
See cases
GPathogenic
ADORA2B, ALKBH5
+240 more
Copy number gain
See cases
GPathogenic
LOC126862516, LOC126862517
+314 more
Copy number loss
See cases
GPathogenic
LOC130060335, LOC130060336
+217 more
Copy number loss
See cases
GPathogenic
ADORA2B, CCDC144A
+64 more
Copy number gain
See cases
GUncertain significance
FAM106C, FAM83G
+311 more
Copy number loss
See cases
GPathogenic
ADORA2B, AKAP10
+311 more
Copy number loss
See cases
GPathogenic
ADORA2B, AKAP10
+311 more
Copy number loss
See cases
GPathogenic
ADORA2B, AKAP10
+311 more
Copy number loss
See cases
GPathogenic
ADORA2B, ALKBH5
+199 more
Copy number loss
See cases
GPathogenic
ALKBH5, ATPAF2
+190 more
Copy number loss
See cases
GPathogenic
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GBenign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
(A180V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
UBB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CENPV, NCOR1
+2 more
Copy number gain
not specified
GUncertain significance
ADORA2B, AKAP10
+61 more
Copy number loss
not specified
GPathogenic
ADORA2B, CCDC144A
+11 more
Copy number gain
not specified
GUncertain significance
ABR, ACADVL
+329 more
Copy number gain
not specified
GPathogenic
ADORA2B, AKAP10
+61 more
Copy number loss
not provided
GPathogenic
CENPV, LRRC75A
+4 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CENPV
+10 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CCDC144A
+10 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CCDC144A
+10 more
Copy number gain
not provided
GUncertain significance
ADORA2B, AKAP10
+78 more
Complex
PMP22-RAI1 contiguous gene duplication syndrome
GPathogenic
CENPV, LRRC75A
+10 more
Copy number gain
not provided
GUncertain significance
UBB, TRPV2
+10 more
Copy number loss
not provided
GUncertain significance
ADORA2B, ALKBH5
+37 more
Copy number loss
not provided
GPathogenic
CCDC144A, CENPV
+7 more
Duplication
not provided
GUncertain significance
ZNF287, CENPV
+9 more
Copy number gain
not provided
GUncertain significance
ZSWIM7, ADORA2B
+10 more
Copy number gain
not provided
GUncertain significance
ADORA2B, ALKBH5
+42 more
Copy number loss
not provided
GPathogenic
ADORA2B, CCDC144A
+10 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CENPV
+9 more
Copy number loss
not provided
GUncertain significance
ADORA2B, CCDC144A
+12 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CENPV
+9 more
Copy number gain
not provided
GUncertain significance
ADORA2B, CCDC144A
+10 more
Copy number gain
See cases
GLikely benign
ALOX12, ALOX12B
+1143 more
Copy number gain
See cases
GPathogenic
SPEM2, TBCD
+1143 more
Copy number gain
See cases
GPathogenic
ADORA2B, AKAP10
+59 more
Copy number loss
See cases
GPathogenic
ADORA2B, AKAP10
+59 more
Copy number gain
See cases
GPathogenic
ADORA2B, ADPRM
+41 more
Complex
Breast ductal adenocarcinoma
GUncertain significance
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