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Items: 18

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHOV
(R130H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHOV
(P127A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHOV
(P101R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(G40S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(A26T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(S25R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(T18P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130056876, RHOV
(P11S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ANKRD63, BAHD1
+49 more
Duplication
Mosaic variegated aneuploidy syndrome 1
GUncertain significance
ACTC1, ADAL
+200 more
Copy number gain
not specified
GPathogenic
C15orf62, DLL4
+9 more
Duplication
not provided
GUncertain significance
CGNL1, MAPDA
+472 more
Duplication
Familial colorectal cancer
+1 more
GUncertain significance
DISP2, C15orf62
+23 more
Copy number gain
not provided
GUncertain significance
CCDC32, RTF1
+60 more
Complex
Spindle cell sarcoma
GPathogenic
PDIA3, PEAK1
+521 more
Duplication
not provided
GPathogenic
AAGAB, ABHD17C
+559 more
Copy number gain
See cases
GPathogenic
NOX5, NPAP1
+559 more
Copy number gain
See cases
GPathogenic
CHRFAM7A, CHRM5
+566 more
Copy number gain
See cases
GPathogenic
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