dbVar for OMIM (Select 600473) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5381510	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914	RNA5SP195, LOC112267855, 174 more genes
nsv4681856	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 139,493,747-139,494,755 , GRCh38.p12 chr5: 140,114,162-140,115,170	PURA
nsv3170342	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr5: 139,493,708-139,499,001 , GRCh38.p12 chr5: 140,114,123-140,119,416	PURA