wbp1[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
nsv3873398	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 20,978,852-20,987,914 , GRCh38 chr1: 20,652,359-20,661,421	DDOST, PINK1-AS
nsv3888954	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 20,973,463-20,978,065 , GRCh38 chr1: 20,646,970-20,651,572	DDOST, PINK1, 1 more genes
nsv4682099	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,688,382-74,692,394 , GRCh38.p12 chr2: 74,461,255-74,465,267	WBP1, MOGS, 1 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	WBP1, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	WBP1, CYP1B1-AS1, 1649 more genes
nsv3877742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551	WBP1, RNU6-561P, 253 more genes
nsv3886532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975	WBP1, RNU6-561P, 249 more genes
nsv6137724	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099	PADI1, RPS15AP6, 176 more genes
nsv3899287	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 15,711,763-21,306,842 , NCBI36 chr1: 15,584,350-21,179,429 , GRCh38 chr1: 15,385,267-20,980,349	EMC1-AS1, TRV-CAC11-2, 166 more genes
nsv4728309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,041,431-21,295,864 , GRCh38.p12 chr1: 15,714,936-20,969,371	RNU1-6P, TRG-CCC4-1, 150 more genes
nsv4728344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 17,284,906-21,778,495 , GRCh38.p12 chr1: 16,958,411-21,452,002	NBL1, AKR7A2, 98 more genes
nsv3890174	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 18,674,315-22,839,387 , NCBI36 chr1: 18,546,902-22,711,974 , GRCh38 chr1: 18,347,821-22,512,894	HTR6, LOC105376817, 103 more genes
nsv7096902	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr2: 71,004,499-74,779,761 , GRCh38.p12 chr2: 70,777,367-74,552,634	WBP1, TAF13P2, 100 more genes
nsv7096907	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 72,359,356-74,779,761 , GRCh38.p12 chr2: 72,132,227-74,552,634	WBP1, RNU6-111P, 71 more genes
nsv3907378	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 20,482,657-21,271,999 , NCBI36 chr1: 20,681,737-21,471,079 , GRCh37 chr1: 20,809,150-21,598,492	RPS4XP4, CAMK2N1, 18 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SNAP47, STK40, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNU1-153P, MIR3917, 4887 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	WBP1, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	WBP1, IGKV2OR2-10, 3737 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 37

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Number of Variants: 20

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