dbVar for OMIM (Select 219800) - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 3,539,741-3,561,489 , GRCh38.p12 chr17: 3,636,447-3,658,195	CTNS, SHPK, 2 more genes
nsv4769293	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 3,547,870-3,554,499 , GRCh38 chr17: 3,644,576-3,651,205	CTNS, CTNS-AS1, 1 more genes
nsv4683059	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 3,558,282-3,558,656 , GRCh38.p12 chr17: 3,654,988-3,655,362	CTNS-AS1, CTNS
nsv4454092	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr17: 3,657,995-3,660,744 , GRCh37 chr17: 3,561,289-3,564,038	CTNS, CTNS-AS1
nsv4453151	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 3,539,712-3,561,479 , GRCh38 chr17: 3,636,418-3,658,185	LOC105371493, CTNS, 2 more genes
nsv4452981	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr17: 3,647,434-3,648,941 , GRCh37 chr17: 3,550,728-3,552,235	LOC105371493, CTNS
nsv4450161	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 3,550,718-3,552,245 , GRCh38 chr17: 3,647,424-3,648,951	CTNS, LOC105371493
nsv3889197	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr17: 3,504,228-3,561,459 , GRCh38 chr17: 3,600,934-3,658,165	CTNS, TRPV1, 4 more genes
nsv3888364	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 3,539,712-3,560,109 , GRCh38 chr17: 3,636,418-3,656,815	CTNS-AS1, CTNS, 2 more genes
nsv3879313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 3,539,712-3,561,489 , GRCh38 chr17: 3,636,418-3,658,195	LOC105371493, CTNS, 2 more genes
nsv3870862	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 3,550,738-3,561,469 , GRCh38 chr17: 3,647,444-3,658,175	CTNS, CTNS-AS1, 1 more genes

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