C1970822[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1622841	NM_080632.3(UPF3B):c.263+5_263+18dup	UPF3B	Duplication (intron variant)	Syndromic X-linked intellectual disability 14 +1 more	GLikely benign
Select item 1562280	NM_080632.3(UPF3B):c.263+9_263+18dup	UPF3B	Duplication (intron variant)	Syndromic X-linked intellectual disability 14	GLikely benign