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Items: 65

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004109, VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
LOC130004109, VCL
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1W
+3 more
GConflicting classifications of pathogenicity
LOC130004109, VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
LOC130004109, VCL
(A45G)
Inversion
(missense variant)
Cardiomyopathy
GUncertain significance
LOC130004109, VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
VCL
(V47G)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
VCL
(V55F)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
VCL
Indel
(intron variant)
Cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
VCL
(R105*)
Single nucleotide variant
(nonsense)
Hypertrophic cardiomyopathy 15
+3 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
VCL
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GConflicting classifications of pathogenicity
VCL
(I135T)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+4 more
GConflicting classifications of pathogenicity
VCL
(K162N)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
VCL
(G167E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
VCL
(T197I)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1W
+4 more
GConflicting classifications of pathogenicity
VCL
(M209L)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
VCL
(M209K)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GBenign/Likely benign
VCL
(L277M)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GBenign/Likely benign
VCL
(L322fs)
Deletion
(frameshift variant)
Cardiomyopathy
GUncertain significance
VCL
(A340V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
VCL
(P347S)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+4 more
GUncertain significance
VCL
(K386R)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+6 more
GConflicting classifications of pathogenicity
VCL
(A413T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GLikely benign
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
VCL
(L432V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
VCL
(I497T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GUncertain significance
VCL
(R512C)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
VCL
(I519L)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+6 more
GConflicting classifications of pathogenicity
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+5 more
GBenign
VCL
(L541V)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+6 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
VCL
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1W
+2 more
GConflicting classifications of pathogenicity
VCL
(S600R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
VCL
Single nucleotide variant
(intron variant)
Cardiomyopathy
GUncertain significance
VCL
(A630T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
VCL
(L682F)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GConflicting classifications of pathogenicity
VCL
(E715K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+2 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
VCL
(R762W)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
VCL
(A803T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
VCL
(R823W)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1W
+1 more
GLikely benign
VCL
(D841H)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+4 more
GConflicting classifications of pathogenicity
VCL
(P847A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+1 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
VCL
(A934V)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+4 more
GBenign/Likely benign
VCL
(P943A)
Single nucleotide variant
(missense variant +1 more)
Primary familial dilated cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
VCL
(M956R)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy
+1 more
GUncertain significance
VCL
(N959H)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GUncertain significance
VCL
(A990V +1 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GUncertain significance
VCL
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
VCL
(E1089D +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GBenign/Likely benign
VCL
(R1049Q +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
VCL
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1W
+1 more
GLikely benign
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