brd3[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
nsv3891679	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 136,932,530-136,933,631 , GRCh38.p12 chr9: 134,067,408-134,068,509	BRD3
nsv3893046	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 136,932,530-136,933,423 , GRCh38.p12 chr9: 134,067,408-134,068,301	BRD3
nsv3891014	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 136,932,556-136,933,423 , GRCh38.p12 chr9: 134,067,434-134,068,301	BRD3
nsv3908384	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 136,876,021-137,005,023 , GRCh38.p12 chr9: 134,010,899-134,139,901	BRD3, WDR5, 3 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	BRD3, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	BRD3, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	BRD3, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	BRD3, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	BRD3, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	BRD3, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	BRD3, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	BRD3, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	BRD3, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	BRD3, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	BRD3, RORB-AS1, 2168 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	BRD3, PGAP4, 2167 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	BRD3, CDRT15P14, 2167 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	BRD3, ABHD17B, 2167 more genes
nsv3892307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,862-141,020,389 , GRCh38.p12 chr9: 203,862-138,125,937	BRD3, PIGO, 2167 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	BRD3, RN7SKP87, 2168 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 45

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Number of Variants: 20

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