Related gene-specific medical variations for Gene (Select 114781) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062923	GRCh37/hg19 6p21.2(chr6:38287197-38317185)x1	BTBD9	Copy number loss	not specified	GUncertain significance
Select item 1809398	GRCh37/hg19 6p21.2(chr6:38454829-38581039)x1	BTBD9	Copy number loss	not provided	GUncertain significance
Select item 686421	GRCh37/hg19 6p21.2(chr6:38140596-38324813)x1	BTBD9	Copy number loss	not provided	GUncertain significance
Select item 686325	GRCh37/hg19 6p21.2(chr6:38174820-38605375)x1	BTBD9	Copy number loss	not provided	GUncertain significance
Select item 563174	GRCh37/hg19 6p21.2(chr6:38454828-38581039)x1	BTBD9	Copy number loss	not provided	GUncertain significance
Select item 562233	Single allele	BTBD9	Deletion	Intellectual disability, mild	GUncertain significance

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