brwd1[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
nsv3896979	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,557,332-40,566,372 , GRCh38.p12 chr21: 39,185,406-39,194,446	BRWD1
nsv3902231	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,557,332-40,566,067 , GRCh38.p12 chr21: 39,185,406-39,194,141	BRWD1
nsv3891035	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,545,790-40,568,528 , GRCh38.p12 chr21: 39,173,864-39,196,602	BRWD1, PSMG1
nsv3903753	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,547,004-40,568,528 , GRCh38.p12 chr21: 39,175,078-39,196,602	BRWD1, PSMG1
nsv3898170	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,546,717-40,567,352 , GRCh38.p12 chr21: 39,174,791-39,195,426	BRWD1, PSMG1
nsv3901521	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,547,329-40,567,352 , GRCh38.p12 chr21: 39,175,403-39,195,426	BRWD1, PSMG1
nsv3907701	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,546,717-40,566,372 , GRCh38.p12 chr21: 39,174,791-39,194,446	BRWD1, PSMG1
nsv3894227	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,547,387-40,566,372 , GRCh38.p12 chr21: 39,175,461-39,194,446	BRWD1, PSMG1
nsv3906910	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,547,329-40,566,067 , GRCh38.p12 chr21: 39,175,403-39,194,141	BRWD1, PSMG1
nsv3904971	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,549,466-40,566,372 , GRCh38.p12 chr21: 39,177,540-39,194,446	BRWD1, PSMG1
nsv3896533	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 40,547,004-40,669,083 , GRCh38.p12 chr21: 39,175,078-39,297,157	BRWD1, TIMM9P2, 2 more genes
nsv3923176	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr21: 7,817,158-46,670,440 , NCBI36 chr21: 14,406,909-46,914,780 , GRCh37 chr21: 15,485,038-48,090,352	BRWD1, COL18A1-AS2, 682 more genes
nsv3905423	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 15,538,655-48,080,926 , GRCh38.p12 chr21: 14,166,334-46,661,014	BRWD1, MTND5P1, 581 more genes
nsv3913105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 36,162,250-48,056,450 , GRCh38 chr21: 34,789,953-46,636,538 , NCBI36 chr21: 35,084,120-46,880,878	BRWD1, KRTAP10-12, 287 more genes
nsv3908171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 37,914,123-48,097,372 , GRCh38.p12 chr21: 36,541,825-46,677,460	BRWD1, AIRE, 256 more genes
nsv3908653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 38,699,545-48,097,372 , GRCh38.p12 chr21: 37,327,243-46,677,460	BRWD1, MIR6070, 239 more genes
nsv3918954	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr21: 37,963,800-46,915,400 , GRCh38 chr21: 37,669,628-46,671,060 , GRCh37 chr21: 39,041,930-48,090,972	BRWD1, LCA5L, 236 more genes
nsv3891817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr21: 34,449,822-43,171,589 , GRCh37 chr21: 35,527,952-44,298,520 , GRCh38.p12 chr21: 34,155,652-42,878,410	BRWD1, LOC107985513, 168 more genes
nsv3923914	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 40,188,323-48,097,372 , NCBI36 chr21: 39,110,193-46,921,800 , GRCh38 chr21: 38,816,399-46,677,460	BRWD1, RNU6-1149P, 219 more genes
nsv4676372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr21: 39,410,438-45,171,756 , GRCh38.p12 chr21: 38,038,136-43,751,875	BRWD1, KCNJ15, 126 more genes

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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

Search results

Items: 1 to 20 of 68

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Number of Variants: 20

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Supplemental Content

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