dbVar for OMIM (Select 305450) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7098565	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,337,406-70,363,304 , GRCh38.p12 chrX: 71,117,556-71,143,454	NLGN3, MED12
nsv7098326	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 70,348,944-70,350,084 , GRCh38.p12 chrX: 71,129,094-71,130,234	MED12
nsv7098325	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 69,748,945-70,644,108 , GRCh38.p12 chrX: 70,529,095-71,424,258	SOCS5P4, SNX12, 23 more genes
nsv7093332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 70,344,187-70,344,188 , GRCh38 chrX: 71,124,337-71,124,338	MED12
nsv5381673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 70,348,958-70,350,070 , GRCh38.p12 chrX: 71,129,108-71,130,220	MED12
nsv5381672	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chrX: 70,338,585-70,362,088 , GRCh38.p12 chrX: 71,118,735-71,142,238	MED12
nsv4683919	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 70,338,595-70,444,419 , GRCh38.p12 chrX: 71,118,745-71,224,569	MED12, LOC107985688, 2 more genes
nsv4681711	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 70,338,595-70,362,078 , GRCh38.p12 chrX: 71,118,745-71,142,228	MED12
nsv3880890	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 71,129,114-71,130,214 , GRCh37 chrX: 70,348,964-70,350,064	MED12

dbVar