dbVar for OMIM (Select 617236) - 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
nsv7148179	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr9: 78,235,965-78,243,734 , GRCh37.p13 chr9: 80,850,881-80,858,650	CEP78
nsv4436066	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr9: 78,228,782-78,244,763 , GRCh37 chr9: 80,843,698-80,859,679	CEP78