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Links from Gene

Items: 1 to 100 of 102

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DUSP4
(P170S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(V281M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(G183R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(T223K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(E91A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(V365I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(A75T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(P155R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(R122Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(I199M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(P178A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4, LOC121331297
(E153K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(I106L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(A267P +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
DUSP4
(H34Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(A341S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM18, ADAM2
+150 more
Copy number gain
not specified
GPathogenic
ADAM18, ADAM2
+234 more
Copy number gain
not specified
GPathogenic
PREX2, PRKDC
+240 more
Copy number gain
not specified
GPathogenic
ADAM28, ADAM7
+39 more
Copy number loss
not specified
GPathogenic
AARD, ABRA
+665 more
Copy number gain
not specified
GPathogenic
ADAM18, ADAM2
+176 more
Copy number gain
not provided
GPathogenic
ADAM28, ADAM7
+145 more
Copy number gain
not provided
GPathogenic
ADAM28, ADAM7
+140 more
Copy number gain
not provided
GPathogenic
SMIM18, SORBS3
+225 more
Copy number gain
not provided
GPathogenic
ADAM18, ADAM2
+180 more
Duplication
not provided
GPathogenic
DUSP4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DUSP4
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DUSP4
(E65Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADAM28, ADAM7
+567 more
Copy number loss
Microcephaly
GPathogenic
DUSP4
(L293V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(P301A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(P79L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(R122W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(R313H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(E107D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(A163G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(V374M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DUSP4
(D180Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADGRA2, ADRB3
+59 more
Copy number loss
not provided
GPathogenic
CDCA2, CLDN23
+250 more
Complex
See cases
GPathogenic
ADAM28, ADAM7
+180 more
Copy number loss
See cases
GPathogenic
ADAMDEC1, ADGRA2
+251 more
Complex
8p inverted duplication/deletion syndrome
GPathogenic
AARD, ABRA
+665 more
Copy number gain
Polydactyly
GPathogenic
SPAG11A, STMN4
+252 more
Copy number gain
Abnormal fetal cardiovascular morphology
GPathogenic
ADAM28, ADAM7
+104 more
Copy number gain
not provided
GLikely pathogenic
BAALC, CNOT7
+665 more
Copy number gain
not provided
GPathogenic
DCTN6, DUSP26
+20 more
Copy number loss
not provided
GUncertain significance
ADAM28, ADAM7
+124 more
Duplication
not provided
GLikely pathogenic
ADAM28, ADAM7
+123 more
Copy number gain
not provided
GLikely pathogenic
ADAM28, ADAM7
+124 more
Copy number gain
not provided
GPathogenic
ASAH1-AS1, ATP6V1B2
+129 more
Copy number gain
See cases
GPathogenic
AARD, ABRA
+593 more
Copy number gain
See cases
GPathogenic
DUSP4, HMBOX1
+2 more
Copy number loss
See cases
GUncertain significance
ADAM18, ADAM2
+186 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+123 more
Copy number gain
See cases
GPathogenic
CCDC25, DUSP4
+14 more
Copy number gain
See cases
GUncertain significance
ADAM18, ADAM28
+151 more
Copy number gain
See cases
GPathogenic
AARD, ABRA
+665 more
Copy number gain
See cases
GPathogenic
FGF20, FGFR1
+665 more
Copy number gain
See cases
GPathogenic
LEPROTL1, LGI3
+109 more
Copy number loss
not provided
Gnot provided
ADRA1A, BNIP3L
+51 more
Copy number gain
See cases
GPathogenic
SCRT1, SCX
+665 more
Copy number gain
See cases
GPathogenic
ADAM18, ADAM2
+180 more
Copy number gain
See cases
GPathogenic
ADAM18, ADAM2
+133 more
Copy number gain
See cases
GUncertain significance
LOC129999967, LOC129999968
+870 more
Copy number gain
See cases
GPathogenic
LOC130000303, LOC130000304
+922 more
Copy number gain
See cases
GPathogenic
LOC124153144, LOC124153145
+818 more
Copy number gain
See cases
GPathogenic
AARD, ABRA
+3663 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+532 more
Copy number loss
See cases
GPathogenic
LOC129999966, LOC129999967
+3111 more
Copy number gain
See cases
GPathogenic
LOC126860438, LOC126860439
+3663 more
Copy number gain
See cases
GPathogenic
LOC130000099, LOC130000100
+1040 more
Copy number gain
See cases
GPathogenic
DPYSL2, DUSP26
+1020 more
Copy number gain
See cases
GPathogenic
LOC113788268, LOC113788269
+929 more
Copy number gain
See cases
GPathogenic
LOC130000050, LOC130000051
+791 more
Copy number gain
See cases
GPathogenic
LOC126860319, LOC126860320
+696 more
Copy number gain
See cases
GPathogenic
LOC129999950, LOC129999951
+996 more
Copy number gain
See cases
GPathogenic
AARD, ABRA
+3661 more
Copy number gain
See cases
GPathogenic
LOC124153126, LOC124153127
+257 more
Copy number loss
See cases
GPathogenic
LOC128772328, LOC129389957
+653 more
Copy number gain
See cases
GPathogenic
LOC130000032, LOC130000033
+1105 more
Copy number gain
See cases
GPathogenic
LOC130000106, LOC130000107
+937 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+567 more
Copy number gain
See cases
GPathogenic
LOC113788272, LOC113788273
+807 more
Copy number gain
See cases
GPathogenic
ADRA1A, BNIP3L
+259 more
Copy number loss
See cases
GPathogenic
KAT6A-AS1, KCNU1
+929 more
Copy number gain
See cases
GPathogenic
LOC130000241, LOC130000242
+934 more
Copy number gain
See cases
GPathogenic
ADRA1A, BNIP3L
+259 more
Copy number loss
See cases
GPathogenic
LOC130000309, LOC130000310
+900 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+523 more
Copy number gain
See cases
GPathogenic
ADAM18, ADAM2
+922 more
Copy number gain
See cases
GPathogenic
LOC130000074, LOC130000075
+929 more
Copy number gain
See cases
GPathogenic
TNFRSF10A, TNFRSF10A-DT
+705 more
Copy number gain
See cases
GPathogenic
AARD, ABRA
+3661 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+979 more
Copy number gain
See cases
GPathogenic
LOC105379224, LOC105379230
+3657 more
Copy number gain
See cases
GPathogenic
ADAM28, ADAM7
+665 more
Copy number gain
See cases
GPathogenic
LOC130000012, LOC130000013
+857 more
Copy number gain
See cases
GPathogenic
LOC130000135, LOC130000136
+593 more
Copy number gain
See cases
GPathogenic
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