dbVar for OMIM (Select 149400) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4454166	copy number variation	2	nstd102	human	Uncertain significance	GRCh38 chr5: 151,892,291-151,924,569 , GRCh37 chr5: 151,271,852-151,304,130	GLRA1
nsv3887607	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr5: 151,924,474-151,924,569 , GRCh37 chr5: 151,304,035-151,304,130	GLRA1
nsv3883509	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 151,234,601-151,304,397 , GRCh38 chr5: 151,855,040-151,924,836	RNA5SP198, TRQ-CTG13-1, 1 more genes