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Links from MedGen

Items: 1 to 100 of 486

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCP
(R50S +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely pathogenic
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(E501G +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
(E685D +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
(F118I +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(P327L +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(V78L +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(G157E +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
(G156V +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
(I392V +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(K658Q +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(M299T +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
(Y134F +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(I82L +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
(P465S +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+2 more
GLikely benign
VCP
Deletion
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+2 more
GConflicting classifications of pathogenicity
VCP
Microsatellite
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(5 prime UTR variant +1 more)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
LOC130001690, VCP
Microsatellite
(5 prime UTR variant +1 more)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
(C77Y +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
(T391I +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
(R745H +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+2 more
GLikely benign
VCP
(R567C +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(G128R +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
(E704A +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
(R211G +1 more)
Single nucleotide variant
(missense variant)
Childhood Onset VCP-related Neurodevelopmental Disorder
+3 more
GLikely pathogenic
VCP
(I196T +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+2 more
GUncertain significance
VCP
(G4E)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+2 more
GUncertain significance
ARID3C, CCL19
+42 more
Duplication
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
ANKRD18B, APTX
+87 more
Duplication
not provided
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(5 prime UTR variant +1 more)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Deletion
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GLikely benign
VCP
(I119V +1 more)
Single nucleotide variant
(missense variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GUncertain significance
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
(R696C +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
(I144V +1 more)
Single nucleotide variant
(missense variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
+1 more
GUncertain significance
VCP
Single nucleotide variant
(synonymous variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
VCP
Single nucleotide variant
(intron variant)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
+1 more
GLikely benign
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