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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935726, LOC129935727
+1665 more
Copy number gain
See cases
GPathogenic
CXCR2
Single nucleotide variant
(intron variant)
not provided
GBenign
CXCR2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CXCR2
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
CXCR2
Single nucleotide variant
(3 prime UTR variant)
not provided
GBenign
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