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Items: 1 to 100 of 28590

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGRN
(K199del +1 more)
Microsatellite
(inframe_deletion)
not provided
+1 more
GUncertain significance
AGRN
(R400W +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
AGRN
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
AGRN
(R1192Q +1 more)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 8
+1 more
GUncertain significance
AGRN
(V1342M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
AGRN
Deletion
(inframe_deletion)
not provided
+1 more
GConflicting classifications of pathogenicity
B3GALT6
(R6Q)
Single nucleotide variant
(missense variant)
not provided
+5 more
GUncertain significance
B3GALT6
(R68fs)
Deletion
(frameshift variant)
Spondyloepimetaphyseal dysplasia with joint laxity
+2 more
GConflicting classifications of pathogenicity
B3GALT6
(F186L)
Single nucleotide variant
(missense variant)
Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
+1 more
GPathogenic
B3GALT6
(E265D)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome, spondylodysplastic type, 2
+2 more
GUncertain significance
B3GALT6
(R302fs)
Duplication
(frameshift variant)
Spondyloepimetaphyseal dysplasia with joint laxity
+2 more
GConflicting classifications of pathogenicity
DVL1
(V644F +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 2
+1 more
GConflicting classifications of pathogenicity
DVL1
(R116Q)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 2
+1 more
GUncertain significance
DVL1
(R40G)
Single nucleotide variant
(missense variant)
Autosomal dominant Robinow syndrome 2
+1 more
GUncertain significance
ATAD3B
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ATAD3A
(P18S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATAD3A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ATAD3A
(R109Q +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ATAD3A
(E111Q +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATAD3A
(A125V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATAD3A
(T280M +2 more)
Single nucleotide variant
(missense variant)
Harel-Yoon syndrome
+1 more
GUncertain significance
ATAD3A
(R424H +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ATAD3A
(E472K +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TMEM240
(V110I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TMEM240
(I12T)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 21
+2 more
GUncertain significance
GNB1
(I80T)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+7 more
GPathogenic/Likely pathogenic
GABRD
(R157Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GABRD
(F269del)
Deletion
(inframe_deletion)
not provided
GUncertain significance
GABRD
(T371M)
Single nucleotide variant
(missense variant)
Idiopathic generalized epilepsy
+1 more
GUncertain significance
GABRD
(V383I)
Single nucleotide variant
(missense variant)
Idiopathic generalized epilepsy
+1 more
GUncertain significance
GABRD
(R408H)
Single nucleotide variant
(missense variant)
Idiopathic generalized epilepsy
+1 more
GUncertain significance
SKI
(R441W)
Single nucleotide variant
(missense variant)
Shprintzen-Goldberg syndrome
+2 more
GConflicting classifications of pathogenicity
SKI
(R519C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PEX10
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
PEX10
Single nucleotide variant
(splice donor variant)
not provided
+3 more
GPathogenic/Likely pathogenic
PEX10
(L297P +4 more)
Single nucleotide variant
(missense variant +1 more)
Peroxisome biogenesis disorder 6A (Zellweger)
+3 more
GConflicting classifications of pathogenicity
PEX10
(L272fs +4 more)
Deletion
(frameshift variant +1 more)
Peroxisome biogenesis disorder
+4 more
GPathogenic
PEX10
(H252fs +4 more)
Deletion
(frameshift variant +1 more)
not provided
+3 more
GPathogenic/Likely pathogenic
PEX10
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
PEX10
(R162Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Peroxisome biogenesis disorder 6A (Zellweger)
+4 more
GUncertain significance
PEX10
Indel
(splice donor variant)
not provided
GLikely pathogenic
PEX10
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
PEX10
(A2S)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
PRDM16
(E271K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CEP104
(A895T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CEP104, LOC126805586
(Q694fs)
Deletion
(frameshift variant)
not provided
GPathogenic
CEP104, LOC126805586
(R631*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic/Likely pathogenic
CEP104, LOC126805587
(I607T)
Single nucleotide variant
(missense variant)
Joubert syndrome 25
+2 more
GConflicting classifications of pathogenicity
CEP104
(E209G)
Single nucleotide variant
(missense variant)
Joubert syndrome 25
+1 more
GConflicting classifications of pathogenicity
CEP104
(S195A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
CEP104
(E184Q)
Single nucleotide variant
(missense variant)
Joubert syndrome 25
+1 more
GConflicting classifications of pathogenicity
NPHP4
Single nucleotide variant
(splice acceptor variant)
not provided
GPathogenic
NPHP4
(V1091M +2 more)
Single nucleotide variant
(missense variant +1 more)
Nephronophthisis
+1 more
GUncertain significance
NPHP4
(A1074P +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
NPHP4
(Q1072* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
NPHP4
(R470W)
Single nucleotide variant
(synonymous variant +2 more)
Senior-Loken syndrome 4
+4 more
GUncertain significance
NPHP4
(A355V)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GUncertain significance
NPHP4
(E223fs)
Deletion
(5 prime UTR variant +2 more)
not provided
GPathogenic
NPHP4
Single nucleotide variant
(splice acceptor variant)
Nephronophthisis
+1 more
GLikely pathogenic
ESPN
(A67V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ESPN
(R113C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ESPN
(V165M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ESPN
(S257N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ESPN
(T676R +2 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
ESPN
(L763V +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ESPN
(V814I +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PLEKHG5
(R956K +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
PLEKHG5
(P695L +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PLEKHG5
Deletion
(inframe_deletion +1 more)
not provided
GUncertain significance
PLEKHG5
(R173Q +2 more)
Single nucleotide variant
(missense variant)
Neuronopathy, distal hereditary motor, autosomal recessive 4
+3 more
GUncertain significance
PLEKHG5
Single nucleotide variant
(splice acceptor variant)
Charcot-Marie-Tooth disease recessive intermediate C
+3 more
GConflicting classifications of pathogenicity
CAMTA1
(A1350V +6 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RERE
(E779D +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
+2 more
GConflicting classifications of pathogenicity
RERE
(A658V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
RERE
(R1146W +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
+1 more
GConflicting classifications of pathogenicity
RERE
(K645del +1 more)
Deletion
(inframe_deletion)
not provided
+1 more
GUncertain significance
RERE
(V233I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
LOC129388438, SLC2A5
(S172R +2 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
H6PD
(Y316* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
PIK3CD
(P231L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PIK3CD
(R271H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PIK3CD
(D707N +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NMNAT1
(F17L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NMNAT1
(N167S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
NMNAT1
(L183F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NMNAT1
(E257K)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic
KIF1B
(P486A +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
KIF1B
(I1090T +1 more)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease type 2A1
+3 more
GConflicting classifications of pathogenicity
TARDBP
(I383V)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
+3 more
GPathogenic/Likely pathogenic
MTOR
(V2291I)
Single nucleotide variant
(missense variant)
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
+1 more
GConflicting classifications of pathogenicity
MTOR
(M1641V +1 more)
Single nucleotide variant
(missense variant)
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
+1 more
GUncertain significance
MTOR
(H1687R)
Single nucleotide variant
(missense variant)
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
+1 more
GConflicting classifications of pathogenicity
MTOR
(G307A)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
DISP3
(Y619fs)
Microsatellite
(frameshift variant)
not provided
GUncertain significance
MTHFR
(R519L +1 more)
Single nucleotide variant
(missense variant)
Neural tube defects, folate-sensitive
+4 more
GConflicting classifications of pathogenicity
MTHFR
(E514fs +1 more)
Microsatellite
(frameshift variant)
not provided
+5 more
GPathogenic/Likely pathogenic
MTHFR
(D223N +1 more)
Single nucleotide variant
(missense variant)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
+2 more
GConflicting classifications of pathogenicity
CLCN6
(Q204R +1 more)
Single nucleotide variant
(missense variant +1 more)
Neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
+1 more
GUncertain significance
PLOD1
(P190L +1 more)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome, kyphoscoliotic type 1
+2 more
GUncertain significance
PLOD1
(G313D +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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