olah[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4449760	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,330,899-32,380,165 , GRCh37 chr13: 32,905,036-32,954,302	BRCA2
nsv3884162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,316,455-32,357,935 , GRCh37 chr13: 32,890,592-32,932,072	BRCA2
nsv3880829	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,316,422-32,355,288 , GRCh37 chr13: 32,890,559-32,929,425	BRCA2
nsv5672565	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,890,592-32,929,431 , GRCh38.p12 chr13: 32,316,455-32,355,294	BRCA2
nsv3871488	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,325,056-32,363,553 , GRCh37 chr13: 32,899,193-32,937,690	BRCA2
nsv4683424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,218-32,937,690 , GRCh38.p12 chr13: 32,326,081-32,363,553	BRCA2
nsv3876256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,232-32,937,676 , GRCh38 chr13: 32,326,095-32,363,539	BRCA2
nsv7094402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,893,194-32,921,053 , GRCh38.p12 chr13: 32,319,057-32,346,916	BRCA2
nsv4682583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,196,977-41,223,340 , GRCh38.p12 chr17: 43,044,960-43,071,323	BRCA1
nsv3879997	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 43,045,677-43,070,927 , GRCh37 chr17: 41,197,694-41,222,944	BRCA1
nsv4683841	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr17: 41,242,941-41,267,816 , GRCh38.p12 chr17: 43,090,924-43,115,799	BRCA1
nsv3887382	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,204,256-41,227,656 , GRCh38 chr17: 43,052,239-43,075,639	BRCA1
nsv5380824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,893,194-32,915,353 , GRCh38.p12 chr13: 32,319,057-32,341,216	BRCA2
nsv4681516	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,197,675-41,219,732 , GRCh38.p12 chr17: 43,045,658-43,067,715	BRCA1
nsv3872021	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,197,694-41,219,711 , GRCh38 chr17: 43,045,677-43,067,694	BRCA1
nsv3881323	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 43,051,118-43,070,927 , GRCh37 chr17: 41,203,135-41,222,944	BRCA1
nsv7095336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,196,353-41,215,988 , GRCh38.p12 chr17: 43,044,336-43,063,971	BRCA1
nsv5672977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,209,048-41,228,651 , GRCh38.p12 chr17: 43,057,031-43,076,634	BRCA1
nsv7095162	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,209,049-41,228,651 , GRCh38.p12 chr17: 43,057,032-43,076,634	BRCA1
nsv1398513	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr17: 41,209,069-41,228,631 , GRCh38 chr17: 43,057,052-43,076,614	BRCA1

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 668

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 668

Page of 34

Number of Variants: 20

Page of 34

Supplemental Content

Find related data

Search details

Recent activity