dbVar for OMIM (Select 106600) - 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
nsv7094251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 37,145,383-37,641,555 , GRCh38.p12 chr14: 36,676,178-37,172,350	MIR4503, LOC107984668, 3 more genes
nsv5380754	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 37,145,383-37,145,677 , GRCh38.p12 chr14: 36,676,178-36,676,472	PAX9, SLC25A21