dbVar for OMIM (Select 202700) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095730	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 852,329-855,814 , GRCh38.p12 chr19: 852,329-855,814 , GRCh38.p12 chr19\|NT_187622.1: 31,216-34,700	ELANE
nsv7095296	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334	ADAMTSL5, GPX4, 90 more genes
nsv5381123	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 852,326-856,164 , GRCh38.p12 chr19: 852,326-856,164 , GRCh38.p12 chr19\|NT_187622.1: 31,213-35,050	ELANE
nsv4682445	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 852,288-856,184 , GRCh38.p12 chr19\|NT_187622.1: 31,175-35,070 , GRCh38.p12 chr19: 852,288-856,184	ELANE
nsv4452856	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 855,938-856,184 , GRCh37 chr19: 855,938-856,184	ELANE