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Items: 42

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC132089226, LOC132089227
+1167 more
Copy number gain
See cases
GPathogenic
MSX2
Insertion
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Single nucleotide variant
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Deletion
not provided
GBenign
MSX2
Deletion
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Duplication
not provided
GBenign
MSX2
Deletion
not provided
GBenign
MSX2
Single nucleotide variant
not provided
GBenign
MSX2
Single nucleotide variant
(5 prime UTR variant)
not provided
+2 more
GBenign
MSX2
(M1V)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely pathogenic
MSX2
Deletion
(inframe_deletion)
not provided
GUncertain significance
MSX2
(A72T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MSX2
Single nucleotide variant
(intron variant)
not provided
GBenign
MSX2
Single nucleotide variant
(intron variant)
not provided
GBenign
MSX2
Single nucleotide variant
(intron variant)
not provided
GBenign
MSX2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MSX2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MSX2
Deletion
(intron variant)
not provided
GLikely benign
MSX2
Microsatellite
(intron variant)
not provided
GLikely benign
MSX2
Microsatellite
(intron variant)
not provided
GBenign
MSX2
Microsatellite
(intron variant)
not provided
GBenign
MSX2
Microsatellite
(intron variant)
not provided
GLikely benign
MSX2
Deletion
(intron variant)
not provided
GLikely benign
MSX2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MSX2
Deletion
not provided
GLikely benign
MSX2
Microsatellite
(intron variant)
not provided
GBenign
MSX2
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
MSX2
Microsatellite
(intron variant)
not provided
GBenign
MSX2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
MSX2
Single nucleotide variant
(intron variant)
not provided
GBenign
MSX2
(M129T)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+4 more
GBenign
MSX2
(F149L)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
MSX2
(R159H)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
MSX2
(E174Q)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
MSX2
(K198E)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
MSX2
(P225S)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
MSX2
(P241R)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
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