dbVar for OMIM (Select 601607) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6137725	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr22: 23,774,226-23,859,697 , GRCh37.p13 chr22: 24,116,413-24,201,884	SMARCB1, MMP11, 2 more genes
nsv5381229	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 24,158,592-24,158,593 , GRCh38 chr22: 23,816,405-23,816,406	SMARCB1
nsv997046	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr22: 23,786,931-23,834,518 , GRCh37 chr22: 24,129,118-24,176,705 , GRCh38.p12 chr22\|NT_187633.1: 23,293-70,880	SMARCB1, DERL3

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dbVar