ClinVar for PubMed (Select 21147883) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2573410	NC_000023.10:g.(?_585078)_(595562_601555)dup	SHOX	Duplication	not specified	GUncertain significance
Select item 1696137	NC_000023.10:g.(595562_601555)_(607559_?)dup	SHOX	Duplication	not specified	GUncertain significance
Select item 929383	GRCh37/hg19 Xp22.33(chrX:434857-979904)x3		Copy number gain	See cases	GLikely pathogenic
Select item 929375	GRCh37/hg19 Xp22.33(chrX:60814-594144)x3		Copy number gain	See cases	GLikely pathogenic
Select item 929356	GRCh37/hg19 Xp22.33(chrX:293493-568604)x3		Copy number gain	See cases	GLikely pathogenic
Select item 929320	GRCh37/hg19 Xp22.33(chrX:578382-1021508)x3		Copy number gain	See cases	GUncertain significance
Select item 560114	Single allele		Duplication	not provided	GUncertain significance
Select item 560099	Single allele		Duplication	not provided	GUncertain significance
Select item 252971	GRCh37/hg19 Xp22.33(chrX:489911-728395)x3		Copy number gain	See cases	GUncertain significance

ClinVar