dbVar for OMIM (Select 233690) - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7094699	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345	HSALR1, LOC105371412, 87 more genes
nsv6310102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,717,354-88,718,353 , GRCh38.p12 chr16: 88,650,946-88,651,945	MVD, CYBA
nsv6310023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,713,499-88,718,353 , GRCh38.p12 chr16: 88,647,091-88,651,945	MVD, CYBA
nsv6310022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,712,514-88,718,096 , GRCh38.p12 chr16: 88,646,106-88,651,688	MVD, CYBA
nsv6137862	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,709,698-88,716,102 , GRCh38.p12 chr16: 88,643,290-88,649,694	CYBA
nsv5673007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,709,737-89,220,635 , GRCh38.p12 chr16: 88,643,329-89,154,227	MIR4722, PIEZO1, 23 more genes
nsv5672933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,713,499-88,714,532 , GRCh38.p12 chr16: 88,647,091-88,648,124	CYBA
nsv4683730	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,709,737-88,714,542 , GRCh38.p12 chr16: 88,643,329-88,648,134	CYBA
nsv4682433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,712,514-88,713,593 , GRCh38.p12 chr16: 88,646,106-88,647,185	CYBA
nsv4681664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,709,737-88,709,989 , GRCh38.p12 chr16: 88,643,329-88,643,581	CYBA
nsv4681487	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 88,709,945-88,713,407 , GRCh38 chr16: 88,643,537-88,646,999	CYBA
nsv4451072	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 88,709,737-88,718,353 , GRCh38 chr16: 88,643,329-88,651,945	MVD, CYBA

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