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
nsv6137657	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 32,921,034-32,968,825 , GRCh38.p12 chr13: 32,346,897-32,394,688	BRCA2, IFIT1P1
nsv6112810	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559	MTUS2, ALOX5AP, 70 more genes
nsv5977925	insertion	1	nstd209	human		GRCh38 chr13: 32,348,302-32,348,302 , GRCh37.p13 chr13: 32,922,439-32,922,439	BRCA2
nsv5946454	copy number variation	1	nstd209	human		GRCh38 chr13: 32,358,204-32,358,519 , GRCh37.p13 chr13: 32,932,341-32,932,656	BRCA2
nsv5706093	mobile element insertion	1	nstd211	human		GRCh38 chr13: 32,392,272-32,392,272 , GRCh37.p13 chr13: 32,966,409-32,966,409	BRCA2
nsv5704931	mobile element insertion	2	nstd211	human		GRCh38 chr13: 32,348,302-32,348,302 , GRCh37.p13 chr13: 32,922,439-32,922,439	BRCA2
nsv5695200	mobile element insertion	1	nstd211	human		GRCh38 chr13: 32,365,742-32,365,742 , GRCh37.p13 chr13: 32,939,879-32,939,879	BRCA2
nsv5674322	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,969,020-32,969,020 , GRCh38 chr13: 32,394,883-32,394,883	BRCA2
nsv5674308	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,937,547-32,937,547 , GRCh38 chr13: 32,363,410-32,363,410	BRCA2
nsv5674294	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,890,642-32,890,642 , GRCh38 chr13: 32,316,505-32,316,505	BRCA2
nsv5674276	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,893,344-32,893,344 , GRCh38 chr13: 32,319,207-32,319,207	BRCA2
nsv5674275	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,953,528-32,953,528 , GRCh38 chr13: 32,379,391-32,379,391	BRCA2
nsv5674270	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,893,288-32,893,288 , GRCh38 chr13: 32,319,151-32,319,151	BRCA2
nsv5674269	delins	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,913,642-32,913,718 , GRCh38 chr13: 32,339,505-32,339,581	BRCA2
nsv5674261	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,913,498-32,913,498 , GRCh38 chr13: 32,339,361-32,339,361	BRCA2
nsv5674253	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,913,888-32,913,888 , GRCh38 chr13: 32,339,751-32,339,751	BRCA2
nsv5674246	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,912,577-32,912,577 , GRCh38 chr13: 32,338,440-32,338,440	BRCA2
nsv5674242	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,912,316-32,912,316 , GRCh38 chr13: 32,338,179-32,338,179	BRCA2
nsv5674240	insertion	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,968,896-32,968,896 , GRCh38 chr13: 32,394,759-32,394,759	BRCA2
nsv5672802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,971,029-32,972,913 , GRCh38.p12 chr13: 32,396,892-32,398,776	BRCA2, N4BP2L1

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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

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Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 485

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Number of Variants: 20

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