dbVar for OMIM (Select 608515) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 183,542,300-183,542,447 , GRCh38.p12 chr1: 183,573,165-183,573,312	NCF2
nsv7095564	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 183,546,714-183,559,464 , GRCh38.p12 chr1: 183,577,579-183,590,329	NCF2, LOC100526839
nsv6310925	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 183,543,602-183,543,776 , GRCh38.p12 chr1: 183,574,467-183,574,641	NCF2
nsv6310922	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 179,520,308-183,559,464 , GRCh38.p12 chr1: 179,551,173-183,590,329	NMNAT2, FAM163A, 78 more genes
nsv4683226	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 183,546,714-183,546,862 , GRCh38.p12 chr1: 183,577,579-183,577,727	NCF2
nsv3874876	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 183,536,035-183,536,500 , GRCh38 chr1: 183,566,900-183,567,365	NCF2