dbVar for OMIM (Select 600211) - dbVar

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Links from OMIM

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7136963	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 45,390,442-45,390,496 , GRCh38 chr6: 45,422,705-45,422,759	RUNX2
nsv3878228	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 45,308,920-45,413,885 , GRCh38 chr6: 45,341,183-45,446,148	RUNX2, SUPT3H