dbVar for OMIM (Select 603553) - 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
nsv5380872	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr10: 72,179,670-72,360,658 , GRCh38.p12 chr10: 70,419,914-70,600,902	NODAL, EIF4EBP2, 3 more genes
nsv4681662	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 72,357,789-72,360,678 , GRCh38.p12 chr10: 70,598,033-70,600,922	PRF1