FANCD - 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
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
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
nsv4728256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,751-32,918,694 , GRCh38.p12 chr13: 32,326,614-32,344,557	BRCA2
nsv3886141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,937,671-32,953,453 , GRCh38 chr13: 32,363,534-32,379,316	BRCA2
nsv4728430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,921,034-32,936,659 , GRCh38.p12 chr13: 32,346,897-32,362,522	BRCA2
nsv5672564	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,890,592-32,905,173 , GRCh38.p12 chr13: 32,316,455-32,331,036	BRCA2
nsv3887430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,715-32,915,032 , GRCh38 chr13: 32,326,578-32,340,895	BRCA2
nsv4728169	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,915,334-32,928,997 , GRCh38.p12 chr13: 32,341,197-32,354,860	BRCA2
nsv3878188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,903,574-32,915,339 , GRCh38 chr13: 32,329,437-32,341,202	BRCA2
nsv7136962	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,918,791-32,928,997 , GRCh38.p12 chr13: 32,344,654-32,354,860	BRCA2
nsv3874095	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,890,592-32,900,425 , GRCh38 chr13: 32,316,455-32,326,288	BRCA2
nsv4682788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,944,519-32,954,302 , GRCh38.p12 chr13: 32,370,382-32,380,165	BRCA2
nsv7098810	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,328,073-32,337,663 , GRCh37 chr13: 32,902,210-32,911,800	BRCA2

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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 1048

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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