ClinVar Miner

List of intergenic variants reported as uncertain significance for Hypertelorism; Global developmental delay; Motor delay; Short chin; Low-set ears; Delayed speech and language development; Depressed nasal bridge; Frontal bossing; Triangular face; Impaired social interactions; Reduced eye contact; Athetosis; Uncontrolled eye movements; Prominent forehead; Hypotonia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
46;XY;ins(7;10)(q32;q22.1q24.3);t(9;16)(q22;q12.1)dn

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