brca1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,760,657-59,934,602 , GRCh38.p12 chr17: 61,683,296-61,857,241	BRIP1
nsv5673137	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,770,781-59,938,900 , GRCh38.p12 chr17: 61,693,420-61,861,539	BRIP1
nsv6310397	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,760,657-59,871,100 , GRCh38.p12 chr17: 61,683,296-61,793,739	BRIP1
nsv7095407	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,760,657-59,861,805 , GRCh38.p12 chr17: 61,683,296-61,784,444	BRIP1
nsv4451993	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 61,715,941-61,808,767 , GRCh37 chr17: 59,793,302-59,886,128	BRIP1
nsv4451754	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 214,728,666-214,797,127 , GRCh37 chr2: 215,593,390-215,661,851	BARD1
nsv5564337	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr2: 215,593,400-215,661,851 , GRCh38.p12 chr2: 214,728,676-214,797,127	BARD1
nsv5381037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,820,364-59,886,128 , GRCh38.p12 chr17: 61,743,003-61,808,767	BRIP1
nsv3883816	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,820,368-59,886,124 , GRCh38 chr17: 61,743,007-61,808,763	BRIP1
nsv5673692	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 215,593,400-215,657,179 , GRCh38.p12 chr2: 214,728,676-214,792,455	BARD1
nsv5672888	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 59,760,657-59,821,962 , GRCh38.p12 chr17: 61,683,296-61,744,601	BRIP1
nsv3878836	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 214,728,670-214,781,515 , GRCh37.p13 chr2: 215,593,394-215,646,239	BARD1
nsv5673378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 215,593,400-215,646,243 , GRCh38.p12 chr2: 214,728,676-214,781,519	BARD1
nsv7098761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,105,163-108,155,884 , GRCh38.p12 chr11: 108,234,436-108,285,157	ATM
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
nsv4453373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,083,875-29,130,719 , GRCh38 chr22: 28,687,887-28,734,731	CHEK2
nsv3881923	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 28,687,891-28,734,727 , GRCh37 chr22: 29,083,879-29,130,715	CHEK2
nsv5673348	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,083,885-29,130,709 , GRCh38.p12 chr22: 28,687,897-28,734,721	CHEK2
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
nsv4451800	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 28,694,022-28,734,731 , GRCh37 chr22: 29,090,010-29,130,719	CHEK2

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Number of Variants: 20

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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 1089

Page of 55

Number of Variants: 20

Page of 55

Supplemental Content

Find related data

Search details

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