dbVar for Gene (Select 5660) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7147103	copy number variation	1	nstd232	human		GRCh37.p13 chr10: 73,579,379-73,579,469 , GRCh38.p12 chr10: 71,819,622-71,819,712	PSAP
nsv7145980	insertion	1	nstd232	human		GRCh37.p13 chr10: 73,591,011-73,591,011 , GRCh38.p12 chr10: 71,831,254-71,831,254	PSAP
nsv7143113	insertion	1	nstd232	human		GRCh37.p13 chr10: 73,579,660-73,579,660 , GRCh38.p12 chr10: 71,819,903-71,819,903	PSAP
nsv7141351	insertion	1	nstd232	human		GRCh37.p13 chr10: 73,587,916-73,587,916 , GRCh38.p12 chr10: 71,828,159-71,828,159	PSAP
nsv7141321	insertion	1	nstd232	human		GRCh37.p13 chr10: 73,577,233-73,577,233 , GRCh38.p12 chr10: 71,817,476-71,817,476	PSAP
nsv7140856	insertion	1	nstd232	human		GRCh37.p13 chr10: 73,580,094-73,580,094 , GRCh38.p12 chr10: 71,820,337-71,820,337	PSAP
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	EXOC6, VCL, 1906 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 more genes
nsv7093891	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,499,381-73,862,745 , GRCh38.p12 chr10: 71,739,624-72,102,987	CDH23, VSIR, 6 more genes
nsv7093798	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,578,585-73,581,640 , GRCh38.p12 chr10: 71,818,828-71,821,883	PSAP
nsv7093797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,464,648-73,768,229 , GRCh38.p12 chr10: 71,704,891-72,008,471	RNU7-38P, CHST3, 5 more genes
nsv6897764	copy number variation	1	nstd229	human		GRCh38 chr10: 71,815,684-71,817,489 , GRCh37.p13 chr10: 73,575,441-73,577,246	PSAP, CDH23
nsv6896443	copy number variation	1	nstd229	human		GRCh38 chr10: 71,832,664-71,906,070 , GRCh37.p13 chr10: 73,592,421-73,665,828	RNU7-38P, PSAP
nsv6892341	copy number variation	1	nstd229	human		GRCh38 chr10: 71,841,612-71,843,948 , GRCh37.p13 chr10: 73,601,369-73,603,705	PSAP, RNU7-38P
nsv6883959	copy number variation	1	nstd229	human		GRCh38 chr10: 71,832,709-72,051,686 , GRCh37.p13 chr10: 73,592,466-73,811,444	PSAP, CHST3, 1 more genes
nsv6883157	copy number variation	1	nstd229	human		GRCh38 chr10: 71,831,194-71,831,337 , GRCh37.p13 chr10: 73,590,951-73,591,094	PSAP
nsv6882834	copy number variation	1	nstd229	human		GRCh38 chr10: 71,831,921-71,834,371 , GRCh37.p13 chr10: 73,591,678-73,594,128	PSAP
nsv6881147	copy number variation	1	nstd229	human		GRCh38 chr10: 71,500,801-71,835,300 , GRCh37.p13 chr10: 73,260,558-73,595,057	LOC105378355, VSIR, 5 more genes
nsv6880342	copy number variation	1	nstd229	human		GRCh38 chr10: 71,756,567-71,978,948 , GRCh37.p13 chr10: 73,516,324-73,738,706	CDH23, MIR7152, 4 more genes
nsv6878978	copy number variation	1	nstd229	human		GRCh38 chr10: 71,849,323-71,849,494 , GRCh37.p13 chr10: 73,609,080-73,609,251	PSAP

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:

Links from Gene

Items: 1 to 20 of 183

Number of Variants: 20

Send to:

Supplemental Content

Find related data

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

Links from Gene

Items: 1 to 20 of 183

Page of 10

Number of Variants: 20

Page of 10

Supplemental Content

Find related data

Recent activity