dbVar for Gene (Select 49) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148281	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 49,757,859-50,740,457 , GRCh37.p13 chr22: 50,151,507-51,178,885	CHKB-CPT1B, ADM2, 49 more genes
nsv7148150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 50,014,114-51,244,066 , GRCh38.p12 chr22: 49,620,466-50,805,638	MAPK11, KLHDC7B-DT, 54 more genes
nsv7065076	inversion	1	nstd229	human		GRCh38 chr22: 50,737,291-50,758,897 , GRCh37.p13 chr22: 51,175,719-51,197,325	ACR, LOC105373100, 2 more genes
nsv7033424	copy number variation	1	nstd229	human		GRCh38 chr22: 50,736,167-50,744,994 , GRCh37.p13 chr22: 51,174,595-51,183,422	ACR, LOC105373100
nsv7024372	copy number variation	1	nstd229	human		GRCh38 chr22: 50,724,051-50,779,604 , GRCh37.p13 chr22: 51,162,479-51,203,353	LOC105373100, SHANK3, 4 more genes
nsv6638073	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,436,847-51,188,164 , GRCh38.p12 chr22: 43,040,841-50,749,736	SCUBE1-AS1, MIR6821, 165 more genes
nsv6638070	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 51,121,376-51,183,840 , GRCh38.p12 chr22: 50,682,948-50,745,412 , GRCh38.p12 chr22\|NW_015148969.1: 19,816-81,523	SHANK3, LOC105373100, 2 more genes
nsv6638058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 51,098,981-51,183,767 , GRCh38.p12 chr22: 50,660,553-50,745,339 , GRCh38.p12 chr22\|NW_015148969.1: 1-81,450	ACR, SHANK3, 2 more genes
nsv6637969	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 44,178,749-51,183,840 , GRCh38.p12 chr22: 43,782,869-50,745,412	LOC105373081, RPL35AP36, 148 more genes
nsv6637710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 45,977,448-51,197,838 , GRCh38.p12 chr22: 45,581,568-50,759,410	PKDREJ, MAPK11, 110 more genes
nsv6637484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 45,977,415-51,183,840 , GRCh38.p12 chr22: 45,581,535-50,745,412	MIR6821, LOC105373086, 108 more genes
nsv6637355	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 45,889,148-51,197,838 , GRCh38.p12 chr22: 45,493,268-50,759,410	LOC105373068, SYCE3, 111 more genes
nsv6542069	copy number variation	1	nstd223	human		GRCh38 chr22: 50,724,709-50,745,442 , GRCh37.p13 chr22: 51,163,137-51,183,870	SHANK3, LOC105373100, 1 more genes
nsv6538725	copy number variation	1	nstd223	human		GRCh38 chr22: 50,740,065-50,740,811 , GRCh37.p13 chr22: 51,178,493-51,179,239	ACR
nsv6535590	copy number variation	1	nstd223	human		GRCh38 chr22: 48,991,693-50,757,224 , GRCh37.p13 chr22: 49,387,505-51,195,652	CHKB-CPT1B, LOC105373096, 57 more genes
nsv6315554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 49,602,454-51,183,869 , GRCh38.p12 chr22: 49,206,528-50,745,441	KLHDC7B-DT, MAPK11, 53 more genes
nsv6315546	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 51,121,452-51,197,838 , GRCh38.p12 chr22: 50,683,024-50,759,410 , GRCh38.p12 chr22\|NW_015148969.1: 19,816-95,522	ACR, SHANK3, 4 more genes
nsv6315282	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 49,883,237-50,740,457 , GRCh37.p13 chr22: 50,276,885-51,178,885	RN7SL500P, IL17REL, 44 more genes
nsv6314059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410	TRABD, LOC100422416, 181 more genes
nsv6313993	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 51,127,903-51,197,838 , GRCh38.p12 chr22: 50,689,475-50,759,410 , GRCh38.p12 chr22\|NW_015148969.1: 25,386-95,522	ACR, SHANK3, 4 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 492

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 492

Page of 25

Number of Variants: 20

Page of 25

Supplemental Content

Find related data

Recent activity