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Items: 1 to 100 of 1119

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NEBL
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
NEBL
Single nucleotide variant
(3 prime UTR variant)
not specified
GBenign
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(F1012L +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GLikely benign
NEBL
(E251K +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
(I1010V +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GBenign/Likely benign
NEBL
(A1007E +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
NEBL
(L1005F +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+2 more
GBenign/Likely benign
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GLikely benign
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
(D223G +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
(D223N +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+2 more
GLikely benign
NEBL
(I243V +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GLikely benign
NEBL
(P206S +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
NEBL
(Q205H +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
(N203D +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(V202A +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
NEBL
(V202I +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+1 more
GLikely benign
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
(D216N +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GLikely benign
NEBL
(G218S +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+1 more
GLikely benign
NEBL
(E228K +6 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Primary dilated cardiomyopathy
+2 more
GUncertain significance
NEBL
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+2 more
GBenign/Likely benign
NEBL
(D209G +6 more)
Single nucleotide variant
(synonymous variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(D225Y +7 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(Q188R +6 more)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
NEBL
(S186I +7 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(Q221*)
Single nucleotide variant
(nonsense +1 more)
Primary dilated cardiomyopathy
GLikely benign
NEBL
(D201N +7 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(R219*)
Single nucleotide variant
(nonsense +1 more)
not provided
+2 more
GLikely benign
NEBL
(Y179C +6 more)
Single nucleotide variant
(synonymous variant +1 more)
NEBL-related disorder
GUncertain significance
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(N175fs +6 more)
Duplication
(frameshift variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(Q188* +6 more)
Single nucleotide variant
(nonsense)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(M170T +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(M170V +6 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Deletion
(inframe_deletion)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(M203I +6 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
NEBL
(M187L +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(V181M +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
+1 more
GBenign/Likely benign
NEBL
(M159K +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
GLikely benign
NEBL
(Y172C +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
NEBL
(Q169E +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(G213A +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(G160R +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
(L211H +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NEBL
Deletion
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
not provided
GBenign
NEBL
Duplication
(intron variant)
not provided
GLikely benign
NEBL
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
(A921P)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant +1 more)
Primary dilated cardiomyopathy
+1 more
GLikely benign
NEBL
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GLikely benign
NEBL
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
NEBL
(P916L)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(T914S)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(V913I)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(E912K)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(C909Y)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
NEBL
(C909R)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
Single nucleotide variant
(synonymous variant +1 more)
Primary dilated cardiomyopathy
+2 more
GLikely benign
NEBL
(S906R)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEBL
(E902K)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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