dbVar for OMIM (Select 601367) - dbVar

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Links from OMIM

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916072	insertion	7	nstd102	human	risk factor, Pathogenic, Benign	GRCh37 chr17: 61,565,892-61,565,892 , GRCh38 chr17: 63,488,531-63,488,531	ACE
nsv3872571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 108,915,663-108,933,582 , GRCh38.p12 chrX: 109,672,434-109,690,353	ACSL4