dbVar for Gene (Select 675) - 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
nsv7137032	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr13: 32,357,845-32,357,846 , GRCh37 chr13: 32,931,982-32,931,983	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
nsv7099000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,953,653-32,954,143 , GRCh38.p12 chr13: 32,379,516-32,380,006	BRCA2
nsv7098952	delins	1	nstd102	human	Likely pathogenic	GRCh38 chr13: 32,376,637-32,376,763 , GRCh37 chr13: 32,950,774-32,950,900	BRCA2
nsv7098864	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 32,906,777-32,907,094 , GRCh38 chr13: 32,332,640-32,332,957	BRCA2
nsv7098820	insertion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr13: 32,379,391-32,379,391 , GRCh37 chr13: 32,953,528-32,953,528	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
nsv7098809	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,952,295-32,957,667 , GRCh38 chr13: 32,378,158-32,383,530	BRCA2, IFIT1P1
nsv7098799	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 32,359,461-32,364,087 , GRCh37 chr13: 32,933,598-32,938,224	BRCA2
nsv7098798	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 32,894,259-32,900,355 , GRCh38 chr13: 32,320,122-32,326,218	BRCA2
nsv7098748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,308,520-32,940,606 , GRCh38.p12 chr13: 31,734,383-32,366,469	BRCA2, FRY, 5 more genes
nsv7098739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,879,403-32,898,814 , GRCh38.p12 chr13: 32,305,266-32,324,677	ZAR1L, BRCA2
nsv7094475	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 32,928,978-32,945,257 , GRCh38.p12 chr13: 32,354,841-32,371,120	BRCA2
nsv7094474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,906,389-32,972,907 , GRCh38.p12 chr13: 32,332,252-32,398,770	N4BP2L1, BRCA2, 1 more genes
nsv7094473	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,218-32,903,649 , GRCh38.p12 chr13: 32,326,081-32,329,512	BRCA2
nsv7094403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,900,616-32,900,770 , GRCh38.p12 chr13: 32,326,479-32,326,633	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
nsv7094401	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 32,893,194-32,903,649 , GRCh38.p12 chr13: 32,319,057-32,329,512	BRCA2
nsv7094400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,889,617-32,903,649 , GRCh38.p12 chr13: 32,315,480-32,329,512	BRCA2, ZAR1L
nsv7094074	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,944,519-32,972,907 , GRCh38.p12 chr13: 32,370,382-32,398,770	N4BP2L1, BRCA2, 1 more genes

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Items: 1 to 20 of 593

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Number of Variants: 20

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