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Items: 43

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004500, LOC130004501
+821 more
Copy number gain
See cases
GPathogenic
EDRF1-AS1, EDRF1-DT
+1036 more
Copy number gain
See cases
GPathogenic
GSTO1, GSTO2
+1097 more
Copy number gain
See cases
GPathogenic
LOC124416905, LOC124416906
+318 more
Copy number loss
See cases
GPathogenic
ABLIM1, ACSL5
+308 more
Copy number loss
See cases
GPathogenic
LOC126861107, LOC128598885
+802 more
Copy number gain
See cases
GPathogenic
ABLIM1, ACSL5
+134 more
Copy number loss
See cases
GLikely pathogenic
ABLIM1, ABRAXAS2
+679 more
Copy number gain
See cases
GPathogenic
LOC130004765, LOC130004766
+109 more
Copy number loss
See cases
GPathogenic
VTI1A
(P64S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(E85K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(L103P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(E148K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(R171C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(R168Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
VTI1A
(S178P +1 more)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
GUncertain significance
VTI1A
(M184I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126861050, LOC126861051
+248 more
Copy number gain
See cases
GLikely pathogenic
VTI1A
(R192C +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
VTI1A
(R199H +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
VTI1A
(V210G +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ABCC2, ABLIM1
+293 more
Copy number gain
not specified
GPathogenic
ABLIM1, ACSL5
+70 more
Copy number gain
not specified
GLikely pathogenic
ACSL5, GPAM
+3 more
Copy number gain
not provided
GUncertain significance
ABLIM1, ABRAXAS2
+117 more
Copy number gain
not provided
GPathogenic
ABLIM1, ABRAXAS2
+145 more
Copy number gain
Distal trisomy 10q
GPathogenic
AGAP5, CRTAC1
+682 more
Copy number gain
Distal trisomy 10q
GPathogenic
ABRAXAS2, CHCHD1
+673 more
Copy number loss
Distal 10q deletion syndrome
GPathogenic
ABLIM1, ABRAXAS2
+146 more
Copy number gain
not specified
GPathogenic
C10orf95, CALHM1
+57 more
Copy number loss
not specified
GPathogenic
ABLIM1, ACSL5
+32 more
Copy number loss
not provided
GUncertain significance
ABLIM1, ABRAXAS2
+130 more
Copy number gain
not provided
GPathogenic
ABLIM1, ABRAXAS2
+146 more
Copy number gain
not provided
GPathogenic
ABCC2, ABLIM1
+298 more
Copy number gain
not provided
GPathogenic
ABLIM1, ABRAXAS2
+157 more
Copy number gain
not provided
GPathogenic
VTI1A, ZDHHC6
Copy number loss
not provided
GLikely benign
COX15, CPEB3
+569 more
Copy number loss
Poly (ADP-Ribose) polymerase inhibitor response
Gdrug response
ABLIM1, ABRAXAS2
+151 more
Copy number gain
See cases
GPathogenic
ABCC2, ABLIM1
+305 more
Copy number gain
See cases
GPathogenic
INA, INPP5A
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+721 more
Copy number gain
See cases
GPathogenic
A1CF, ABCC2
+722 more
Copy number gain
See cases
GPathogenic
ABLIM1, ABRAXAS2
+201 more
Copy number gain
See cases
GPathogenic
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