dbVar for OMIM (Select 609628) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095437	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 2,656,075-2,960,838 , GRCh38.p12 chr18: 2,656,076-2,960,840	LPIN2, EMILIN2, 2 more genes
nsv6310356	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 2,920,291-3,457,938 , GRCh38.p12 chr18: 2,920,293-3,457,940	LOC101927044, LPIN2, 14 more genes
nsv6310256	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 2,920,291-2,940,730 , GRCh38.p12 chr18: 2,920,293-2,940,732	LPIN2
nsv5672990	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr18: 2,921,511-2,938,055 , GRCh38.p12 chr18: 2,921,513-2,938,057	LPIN2
nsv5381045	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 2,920,271-2,931,461 , GRCh38.p12 chr18: 2,920,273-2,931,463	LPIN2
nsv4683608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 2,931,234-2,951,374 , GRCh38.p12 chr18: 2,931,236-2,951,376	LPIN2, CHORDC1P4
nsv4682412	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 2,926,701-2,929,176 , GRCh38.p12 chr18: 2,926,703-2,929,178	LPIN2
nsv3888681	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr18: 2,921,533-2,938,037 , GRCh37.p13 chr18: 2,921,531-2,938,035	LPIN2
nsv3879767	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh38 chr18: 2,920,273-2,960,860 , GRCh37 chr18: 2,920,271-2,960,858	LPIN2, CHORDC1P4

dbVar