dbVar for OMIM (Select 270400) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112744	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 71,155,018-71,156,024 , GRCh38.p12 chr11: 71,443,972-71,444,978	DHCR7
nsv5672638	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 71,146,411-71,152,496 , GRCh38.p12 chr11: 71,435,365-71,441,450	DHCR7
nsv5672637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,146,411-71,146,895 , GRCh38.p12 chr11: 71,435,365-71,435,849	DHCR7
nsv4683128	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,152,263-71,152,496 , GRCh38.p12 chr11: 71,441,217-71,441,450	DHCR7
nsv4683017	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,155,029-71,156,008 , GRCh38.p12 chr11: 71,443,983-71,444,962	DHCR7
nsv4681998	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,152,263-71,156,008 , GRCh38.p12 chr11: 71,441,217-71,444,962	DHCR7