rad52[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
nsv6290211	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 1,034,616-1,086,272 , GRCh38.p12 chr12: 925,450-977,106	RAD52
nsv6290477	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 879,711-984,377 , GRCh37.p13 chr12: 988,877-1,093,543	RAD52, WNK1
nsv4456327	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 988,557-1,081,509 , GRCh38.p12 chr12: 879,391-972,343	RAD52, WNK1
nsv3900500	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 1,047,531-1,441,137 , GRCh38.p12 chr12: 938,365-1,331,971	RAD52, ERC1, 1 more genes
nsv4675609	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 1,024,418-1,401,311 , GRCh38.p12 chr12: 915,252-1,292,145	RAD52, HTR1DP1, 1 more genes
nsv3891584	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 1,098,614-1,366,110 , GRCh38.p12 chr12: 989,448-1,256,944	RAD52, ERC1, 1 more genes
nsv3913771	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 881,990-1,327,038 , GRCh37.p13 chr12: 1,011,729-1,456,777 , GRCh38.p12 chr12: 902,563-1,347,611	RAD52, HTR1DP1, 3 more genes
nsv3924127	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 936,769-1,244,917 , NCBI36 chr12: 916,196-1,224,344 , GRCh37 chr12: 1,045,935-1,354,083	RAD52, HTR1DP1, 1 more genes
nsv3900268	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 915,106-1,577,381 , GRCh38.p12 chr12: 805,940-1,468,215	RAD52, WNK1, 3 more genes
nsv4456684	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 1,019,260-1,562,637 , GRCh38.p12 chr12: 910,094-1,453,471	RAD52, WNK1, 3 more genes
nsv4729196	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 1,015,338-1,518,434 , GRCh38.p12 chr12: 906,172-1,409,268	RAD52, HTR1DP1, 3 more genes
nsv6637869	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 1,037,077-1,487,331 , GRCh38.p12 chr12: 927,911-1,378,165	RAD52, LOC107987182, 2 more genes
nsv3916470	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 881,990-1,287,038 , GRCh37.p13 chr12: 1,011,729-1,416,777 , GRCh38.p12 chr12: 902,563-1,307,611	RAD52, ERC1, 2 more genes
nsv3919337	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 881,953-1,258,773 , GRCh38 chr12: 902,526-1,279,346 , GRCh37 chr12: 1,011,692-1,388,512	RAD52, ERC1, 2 more genes
nsv4675274	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 937,798-1,289,250 , GRCh38.p12 chr12: 828,632-1,180,084	RAD52, HTR1DP1, 2 more genes
nsv3896736	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 873,649-1,074,732 , GRCh38.p12 chr12: 764,483-965,566	RAD52, WNK1, 1 more genes
nsv4455308	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 982,093-1,115,007 , GRCh38.p12 chr12: 872,927-1,005,841	RAD52, ERC1, 1 more genes
nsv4457052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926	RAD52, TSPAN9, 118 more genes
nsv3906935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,201,932 , GRCh38.p12 chr12: 64,620-6,092,766	RAD52, LRTM2, 113 more genes
nsv3907924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,039,841 , GRCh38.p12 chr12: 64,620-5,930,675	RAD52, SLC6A13, 111 more genes

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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 89

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Number of Variants: 20

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