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Items: 1 to 100 of 1724

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCG5, ABCG8
+1631 more
Copy number gain
See cases
GPathogenic
ABCG5, ABCG8
+1400 more
Copy number gain
See cases
GPathogenic
LOC126806252, LOC126806253
+2457 more
Copy number gain
See cases
GBenign
ARHGEF33, ATL2
+154 more
Copy number loss
See cases
GPathogenic
ARHGEF33, SOS1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ARHGEF33, SOS1
Single nucleotide variant
(intron variant)
not provided
GLikely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GBenign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign
SOS1
Deletion
(3 prime UTR variant)
not provided
GBenign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+2 more
GBenign/Likely benign
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+1 more
GLikely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Gingival fibromatosis
+4 more
GLikely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+4 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
not provided
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Deletion
(3 prime UTR variant)
Gingival fibromatosis
+4 more
GLikely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Duplication
(3 prime UTR variant)
Noonan syndrome 4
+4 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Microsatellite
(3 prime UTR variant)
Gingival fibromatosis
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GBenign/Likely benign
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign
SOS1
Deletion
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Fibromatosis, gingival, 1
+2 more
GConflicting classifications of pathogenicity
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
SOS1
Single nucleotide variant
(3 prime UTR variant)
Noonan syndrome 4
+1 more
GUncertain significance
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