ClinVar for MedGen (Select 411727) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235933	GRCh38/hg38 Xq28(chrX:154895862-155336084)	BRCC3, CLIC2 +34 more	Copy number gain	Chromosome Xq28 duplication syndrome	GPathogenic
Select item 3066030	NC_000023.11:g.153670446_154329698dup	ABCD1, ARHGAP4 +59 more	Duplication	Chromosome Xq28 duplication syndrome	GPathogenic
Select item 2580330	GRCh37/hg19 Xq28(chrX:153247464-153522710)x3	IRAK1, MECP2 +5 more	Copy number gain	Chromosome Xq28 duplication syndrome	GPathogenic
Select item 2572018	GRCh37/hg19 Xq28(chrX:153566798-153748208)x4	ATP6AP1, DNASE1L1 +11 more	Copy number gain	Chromosome Xq28 duplication syndrome	Gnot provided
Select item 1703536	GRCh37/hg19 Xq28(chrX:152372767-155233731)	CLIC2, CMC4 +68 more	Copy number gain	Chromosome Xq28 duplication syndrome +1 more	GPathogenic
Select item 1339850	GRCh37/hg19 Xq28(chrX:154124170-154528181)x3	BRCC3, CLIC2 +6 more	Copy number gain	Chromosome Xq28 duplication syndrome	Gnot provided
Select item 1162265	NC_000023.11:g.(?_144988272)_(145271978_?)dup	SPANXN1	Duplication	Chromosome Xq28 duplication syndrome	GUncertain significance
Select item 1065195	GRCh38/hg38 Xq28(chrX:153858452-154332213)x2	ARHGAP4, AVPR2 +41 more	Copy number gain	Chromosome Xq28 duplication syndrome	GPathogenic

ClinVar