dbVar for OMIM (Select 103850) - 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
nsv5564226	copy number variation	7	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr16: 29,802,081-30,199,917 , GRCh38.p12 chr16: 29,790,760-30,188,596	MAPK3, MAZ, 27 more genes
nsv3872596	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 30,066,083-30,081,533 , GRCh38 chr16: 30,054,762-30,070,212	LOC112694756, ALDOA