U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from Gene

Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CXCR6, FYCO1
(F29I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(G313E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(V209I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(E94G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(R254C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ALS2CL, ARIH2
+66 more
Duplication
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome
GUncertain significance
CXCR6, FYCO1
(T66M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(G107D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(L283F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CXCR6, FYCO1
(T337P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NCKIPSD, NDUFAF3
+71 more
Copy number loss
not provided
GPathogenic
CCR9, CXCR6
+3 more
Duplication
not provided
GUncertain significance
CXCR6, FYCO1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CXCR6, FYCO1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
CXCR6, FYCO1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
CCR9, CXCR6
+3 more
Copy number gain
not provided
GUncertain significance
APEH, HEMK1
+177 more
Copy number gain
not provided
GPathogenic
HHLA2, HIGD1A
+1054 more
Copy number gain
See cases
GPathogenic
A4GNT, AADAC
+1054 more
Copy number gain
See cases
GPathogenic
ABHD5, ACAA1
+177 more
Copy number gain
See cases
GLikely pathogenic
CCR1, CCR3
+23 more
Copy number gain
See cases
GLikely benign
ALS2CL, AMIGO3
+379 more
Copy number gain
See cases
GPathogenic
Format
Items per page
Sort by
Choose Destination