brpf1[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
nsv4578449	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 9,783,709-9,786,192 , GRCh38.p12 chr3: 9,742,025-9,744,508	BRPF1
nsv3905232	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982	BRPF1, OR7E122P, 163 more genes
nsv3885461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910	BRPF1, MARK2P14, 160 more genes
nsv6636276	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035	BRPF1, RPL23AP39, 144 more genes
nsv3906827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309	BRPF1, LOC107986040, 142 more genes
nsv3895550	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288	BRPF1, SRGAP3, 141 more genes
nsv3900952	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255	BRPF1, RPUSD3, 137 more genes
nsv3900980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-10,672,995 , GRCh38 chr3: 32,241-10,631,310 , NCBI36 chr3: 48,914-10,647,995	BRPF1, MIR885, 131 more genes
nsv3892568	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 705,581-11,067,828 , GRCh37 chr3: 730,581-11,092,828 , GRCh38 chr3: 688,897-11,051,142	BRPF1, DUSP5P2, 126 more genes
nsv3894686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 48,914-10,339,808 , GRCh38 chr3: 32,241-10,323,124 , GRCh37 chr3: 73,914-10,364,808	BRPF1, RPL21P17, 128 more genes
nsv4674715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141	BRPF1, LOC105376944, 122 more genes
nsv3889023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,104,842 , GRCh38.p12 chr3: 20,213-10,063,158	BRPF1, TTLL3, 118 more genes
nsv6636296	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921	BRPF1, GRM7-AS1, 101 more genes
nsv6313525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410	BRPF1, EGOT, 95 more genes
nsv3900214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300	TYMP, MIR4535, 218 more genes
nsv6290298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638	CERK, LINC01315, 212 more genes
nsv3912011	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264	TUBGCP6, MAPK12, 213 more genes
nsv5381149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300	WBP2NL, RN7SKP80, 210 more genes
nsv4351202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331	PLXNB2, WBP2NL, 204 more genes
nsv3893572	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410	CYP2D8P, CYP2D6, 206 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 195

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Number of Variants: 20

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