dbVar for Gene (Select 3098) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7146207	insertion	1	nstd232	human		GRCh37.p13 chr10: 71,139,853-71,139,853 , GRCh38.p12 chr10: 69,380,097-69,380,097	HK1
nsv7142108	insertion	1	nstd232	human		GRCh37.p13 chr10: 71,119,801-71,119,801 , GRCh38.p12 chr10: 69,360,045-69,360,045	HK1
nsv7139592	insertion	1	nstd232	human		GRCh37.p13 chr10: 71,146,175-71,146,175 , GRCh38.p12 chr10: 69,386,419-69,386,419	HK1
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
nsv7093795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 71,038,467-71,160,891 , GRCh38.p12 chr10: 69,278,711-69,401,135	RPS15AP28, HK1
nsv7093724	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 71,075,744-71,103,765 , GRCh38.p12 chr10: 69,315,988-69,344,009	HK1
nsv7093643	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 71,103,563-71,103,765 , GRCh38.p12 chr10: 69,343,807-69,344,009	HK1
nsv6897749	copy number variation	1	nstd229	human		GRCh38 chr10: 69,318,201-69,319,600 , GRCh37.p13 chr10: 71,077,957-71,079,356	HK1
nsv6896431	copy number variation	1	nstd229	human		GRCh38 chr10: 69,283,177-69,287,451 , GRCh37.p13 chr10: 71,042,933-71,047,207	HK1
nsv6895886	copy number variation	1	nstd229	human		GRCh38 chr10: 69,307,470-69,315,582 , GRCh37.p13 chr10: 71,067,226-71,075,338	HK1
nsv6895499	copy number variation	1	nstd229	human		GRCh38 chr10: 69,299,080-69,299,593 , GRCh37.p13 chr10: 71,058,836-71,059,349	RPS15AP28, HK1
nsv6895482	copy number variation	1	nstd229	human		GRCh38 chr10: 69,297,618-69,300,786 , GRCh37.p13 chr10: 71,057,374-71,060,542	HK1, RPS15AP28
nsv6895165	copy number variation	1	nstd229	human		GRCh38 chr10: 69,395,105-69,400,988 , GRCh37.p13 chr10: 71,154,861-71,160,744	HK1
nsv6894502	copy number variation	1	nstd229	human		GRCh38 chr10: 69,293,474-69,304,988 , GRCh37.p13 chr10: 71,053,230-71,064,744	RPS15AP28, HK1
nsv6891721	copy number variation	1	nstd229	human		GRCh38 chr10: 69,234,052-69,336,830 , GRCh37.p13 chr10: 70,993,808-71,096,586	HK1, RPS15AP28, 1 more genes
nsv6890815	copy number variation	1	nstd229	human		GRCh38 chr10: 69,351,128-69,354,886 , GRCh37.p13 chr10: 71,110,884-71,114,642	HK1
nsv6889988	copy number variation	1	nstd229	human		GRCh38 chr10: 69,287,201-69,290,725 , GRCh37.p13 chr10: 71,046,957-71,050,481	HK1
nsv6888604	copy number variation	1	nstd229	human		GRCh38 chr10: 69,264,254-69,277,928 , GRCh37.p13 chr10: 71,024,010-71,037,684	HKDC1, HK1
nsv6887931	copy number variation	1	nstd229	human		GRCh38 chr10: 69,232,301-69,362,300 , GRCh37.p13 chr10: 70,992,057-71,122,056	HK1, LOC101928994, 2 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:

Links from Gene

Items: 1 to 20 of 443

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 443

Page of 23

Number of Variants: 20

Page of 23

Supplemental Content

Find related data

Recent activity