prx[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
nsv3887000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 40,909,593-40,909,789 , GRCh38 chr19: 40,403,686-40,403,882	PRX
nsv4683466	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 40,909,603-40,909,779 , GRCh38.p12 chr19: 40,403,696-40,403,872	PRX
nsv6635984	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 40,902,692-40,902,769 , GRCh38 chr19: 40,396,785-40,396,862	PRX
nsv4681045	copy number variation	3	nstd102	human	Uncertain significance	GRCh38 chr19: 40,396,707-40,396,784 , GRCh37 chr19: 40,902,614-40,902,691	PRX
nsv4454769	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 40,393,956-40,407,942 , GRCh37 chr19: 40,899,863-40,913,849	PRX
nsv7095279	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 40,899,873-40,904,743 , GRCh38.p12 chr19: 40,393,966-40,398,836	PRX
nsv7093038	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 40,396,228-40,396,229 , GRCh37 chr19: 40,902,135-40,902,136	PRX
nsv6310453	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 40,396,138-40,396,139 , GRCh37 chr19: 40,902,045-40,902,046	PRX
nsv5381266	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 40,902,613-40,902,614 , GRCh38 chr19: 40,396,706-40,396,707	PRX
nsv3898794	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 168,525,390-168,991,920 , GRCh38 chr1: 170,289,625-170,756,155 , GRCh37 chr1: 170,258,766-170,725,296	GORAB-AS1, GORAB, 3 more genes
nsv4728742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 170,503,528-170,666,132 , GRCh38.p12 chr1: 170,534,387-170,696,991	PRRX1, LOC105371610, 1 more genes
nsv4728659	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 173,377,818-173,495,656 , GRCh38.p12 chr1: 173,408,679-173,526,517	SLC9C2, TNFSF4, 3 more genes
nsv3893836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 23,383,292-23,717,368 , GRCh38 chrX: 23,365,175-23,699,251 , NCBI36 chrX: 23,293,213-23,627,289	PRDX4, PTCHD1, 1 more genes
nsv3885416	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 23,550,048-23,825,483 , GRCh38.p12 chrX: 23,531,931-23,807,366	SAT1-DT, SAT1, 2 more genes
nsv4454258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 170,519,336-170,666,165 , GRCh38.p12 chr1: 170,550,195-170,697,024	LOC105371610, PRRX1, 1 more genes
nsv4455299	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 120,909,427-121,024,166 , GRCh38.p12 chr10: 119,149,915-119,264,654	PRDX3, SFXN4, 3 more genes
nsv4456176	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 120,933,323-121,007,499 , GRCh38.p12 chr10: 119,173,811-119,247,987	GRK5-IT1, RN7SL749P, 2 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	NANOGNBP3, PRXL2CP1, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	NHS-AS1, DUSP21, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	GPR119, RN7SKP81, 2153 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 262

Page of 14

Number of Variants: 20

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