pros1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6311886	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,605,147-93,617,433 , GRCh38.p12 chr3: 93,886,303-93,898,589	PROS1
nsv3876895	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,879,163-93,879,314 , GRCh37 chr3: 93,598,007-93,598,158	PROS1
nsv6290197	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr3: 93,879,713-93,906,171 , GRCh37.p13 chr3: 93,598,557-93,625,015	PROS1
nsv7096478	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 93,646,084-93,647,651 , GRCh38.p12 chr3: 93,927,240-93,928,807	PROS1
nsv3882516	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,612,369-93,641,533 , GRCh38.p12 chr3: 93,893,525-93,922,689	PROS1
nsv4683992	insertion	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,593,087-93,593,087 , GRCh38 chr3: 93,874,243-93,874,243	PROS1
nsv6311701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,629,453-93,692,783 , GRCh38.p12 chr3: 93,910,609-93,973,939	PROS1, HSPE1P17
nsv4682090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,643,074-93,692,783 , GRCh38.p12 chr3: 93,924,230-93,973,939	PROS1, HSPE1P17
nsv4451750	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 93,591,831-93,692,960 , GRCh38.p12 chr3: 93,872,987-93,974,116	PROS1, HSPE1P17
nsv3878587	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,537,290-93,645,047 , GRCh38.p12 chr3: 93,818,446-93,926,203	PROS1, RNU6-488P
nsv3884309	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 93,519,464-93,600,241 , GRCh38.p12 chr3: 93,800,620-93,881,397	PROS1, RNU6-488P
nsv3920595	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 90,394,654-95,159,858 , GRCh37.p13 chr3: 90,311,964-93,677,168 , GRCh38.p12 chr3: 90,262,814-93,958,324	PROS1, HSPE1P17, 2 more genes
nsv3924898	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,519,465-93,674,112 , NCBI36 chr3: 95,002,155-95,156,802 , GRCh38 chr3: 93,800,621-93,955,268	PROS1, HSPE1P17, 1 more genes
nsv6311806	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,593,089-93,722,772 , GRCh38.p12 chr3: 93,874,245-94,003,928	PROS1, RNU6-511P, 3 more genes
nsv7096479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,692,478-93,699,346 , GRCh38.p12 chr3: 93,973,634-93,980,502	PROS1, ARL13B, 1 more genes
nsv6311807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,593,089-93,845,334 , GRCh38.p12 chr3: 93,874,245-94,126,490	PROS1, NSUN3, 7 more genes
nsv3886942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,593,083-93,772,112 , GRCh38 chr3: 93,874,239-94,053,268	PROS1, ARL13B, 4 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	PROS1, MTCO2P29, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	PROS1, ATP6V1A, 297 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	PROS1, RNU4-62P, 2880 more genes

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

Send to:

Search results

Items: 1 to 20 of 41

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 41

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity