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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129933244, LOC129933245
+653 more
Copy number gain
See cases
GPathogenic
LOC126806103, LOC126806104
+1047 more
Copy number gain
See cases
GPathogenic
LOC129933186, LOC129933187
+736 more
Copy number gain
See cases
GPathogenic
ABHD1, ACP1
+893 more
Copy number gain
See cases
GPathogenic
LOC129933311, LOC129933312
+1631 more
Copy number gain
See cases
GPathogenic
LINC01115, LINC01121
+1400 more
Copy number gain
See cases
GPathogenic
HAAO, HADHA
+2457 more
Copy number gain
See cases
GBenign
TRY-GTA2-1, UBXN2A
+321 more
Copy number loss
See cases
GPathogenic
ATAD2B, FAM228B
+19 more
Copy number loss
See cases
GUncertain significance
UBXN2A
(V15I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(G19V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(S31P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(N32Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(A55T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
UBXN2A
(D112N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(V113I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(T126A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(T126M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(P128L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(V156I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(I192F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(H194R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UBXN2A
(E255G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ABHD1, ACP1
+182 more
Copy number gain
See cases
GPathogenic
ATAD2B, FAM228A
+10 more
Copy number gain
not provided
GUncertain significance
ABHD1, ADAM17
+177 more
Copy number gain
not provided
GPathogenic
ACTG2, ACTR1B
+529 more
Copy number loss
See cases
GPathogenic
ABCA12, ABCB11
+1216 more
Copy number gain
Mosaic trisomy 2
GPathogenic
FAM228A, FAM228B
+19 more
Copy number loss
2p24.1p23.3 microdeletion syndrome
GPathogenic
APOB, ATAD2B
+22 more
Copy number loss
not provided
GPathogenic
FKBP1B, UBXN2A
+3 more
Copy number loss
not provided
GUncertain significance
RGPD4, RGPD5
+1214 more
Copy number gain
See cases
GPathogenic
IL1F10, IL1R1
+1214 more
Copy number gain
See cases
GPathogenic
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