dbVar for OMIM (Select 300823) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3874002	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 149,478,764-149,505,354 , GRCh37.p13 chrX\|NW_004070890.2: 5,003,162-5,029,752 , GRCh37.p13 chrX: 148,560,295-148,586,884	IDS
nsv997161	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 148,558,521-148,586,884 , GRCh38.p12 chrX: 149,476,990-149,505,354	IDS