"nstd165"[study] AND "deletion"[variant_type] - dbVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

loading data ...

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3565987	copy number variation	1	nstd165	human	GRCh37 chr17: 41,201,138-41,209,152 , GRCh38.p12 chr17: 43,049,121-43,057,135	BRCA1
nsv3565988	copy number variation	1	nstd165	human	GRCh37 chr17: 41,219,625-41,223,255 , GRCh38.p12 chr17: 43,067,608-43,071,238	BRCA1
nsv3565986	copy number variation	1	nstd165	human	GRCh37 chr13: 32,968,923-32,972,466 , GRCh38.p12 chr13: 32,394,786-32,398,329	BRCA2
nsv3565983	copy number variation	1	nstd165	human	GRCh37 chr13: 32,930,565-32,932,066 , GRCh38.p12 chr13: 32,356,428-32,357,929	BRCA2
nsv3565985	copy number variation	1	nstd165	human	GRCh37 chr13: 32,936,660-32,936,830 , GRCh38.p12 chr13: 32,362,523-32,362,693	BRCA2
nsv4345826	copy number variation	1	nstd165	human	GRCh37 chr17: 41,197,701-41,197,781 , GRCh38.p12 chr17: 43,045,684-43,045,764	BRCA1
nsv3565984	copy number variation	1	nstd165	human	GRCh37 chr13: 32,936,660-32,936,728 , GRCh38.p12 chr13: 32,362,523-32,362,591	BRCA2