Related gene-specific medical variations for Gene (Select 6907) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2497741	NM_005647.4(TBL1X):c.373G>A (p.Asp125Asn)	TBL1X (D125N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 687654	GRCh37/hg19 Xp22.31-22.2(chrX:9477864-9534569)x0	TBL1X	Copy number loss	not provided	GUncertain significance
Select item 564778	GRCh37/hg19 Xp22.31-22.2(chrX:9069878-9527470)x2	TBL1X	Copy number gain	not provided	GUncertain significance

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