dbVar for OMIM (Select 604370) - 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
nsv3913353	insertion	1	nstd102	human	Uncertain significance	GRCh37 chr17: 41,209,021-41,209,021 , GRCh38 chr17: 43,057,004-43,057,004	BRCA1
nsv3913299	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,243,705-41,243,709 , GRCh38 chr17: 43,091,688-43,091,692	BRCA1
nsv3913224	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,242,990-41,242,990 , GRCh38 chr17: 43,090,973-43,090,973	BRCA1
nsv3913104	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,246,696-41,246,696 , GRCh38 chr17: 43,094,679-43,094,679	BRCA1
nsv3912436	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,197,724-41,197,724 , GRCh38 chr17: 43,045,707-43,045,707	BRCA1
nsv3911810	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,245,043-41,245,043 , GRCh38 chr17: 43,093,026-43,093,026	BRCA1
nsv3911709	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,228,600-41,228,600 , GRCh38 chr17: 43,076,583-43,076,583	BRCA1
nsv3911558	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,244,495-41,244,495 , GRCh38 chr17: 43,092,478-43,092,478	BRCA1
nsv3911547	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,210,171-41,217,415 , GRCh38 chr17: 43,058,154-43,065,398	BRCA1
nsv3911267	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,222,943-41,222,943 , GRCh38 chr17: 43,070,926-43,070,926	BRCA1
nsv3911196	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,246,740-41,246,740 , GRCh38 chr17: 43,094,723-43,094,723	BRCA1
nsv3911069	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,275,786-41,276,180 , GRCh38 chr17: 43,123,769-43,124,163	BRCA1, NBR2
nsv3910333	delins	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 41,197,742-41,197,744 , GRCh38 chr17: 43,045,725-43,045,727	BRCA1
nsv3910318	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,245,863-41,245,911 , GRCh38 chr17: 43,093,846-43,093,894	BRCA1
nsv3909868	insertion	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,234,439-41,234,439 , GRCh38 chr17: 43,082,422-43,082,422	BRCA1
nsv3889892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,228,632-41,276,114 , GRCh38 chr17: 43,076,615-43,124,097	BRCA1, RPL21P4, 1 more genes
nsv3889751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,276,133-41,277,500 , GRCh38 chr17: 43,124,116-43,125,483	BRCA1, NBR2
nsv3889685	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 43,099,881-43,125,483 , GRCh37 chr17: 41,251,898-41,277,500	BRCA1, NBR2
nsv3889642	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,234,593-41,277,500 , GRCh38 chr17: 43,082,576-43,125,483	NBR2, BRCA1
nsv3888898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 41,228,505-41,228,631 , GRCh38 chr17: 43,076,488-43,076,614	BRCA1

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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

Links from OMIM

Items: 1 to 20 of 98

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Number of Variants: 20

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Supplemental Content

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Recent activity