dbVar for Gene (Select 8013) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5965927	insertion	1	nstd209	human		GRCh38 chr9: 99,862,549-99,862,549 , GRCh37.p13 chr9: 102,624,831-102,624,831	NR4A3
nsv5918920	copy number variation	1	nstd209	human		GRCh38 chr9: 99,828,561-99,828,680 , GRCh37.p13 chr9: 102,590,843-102,590,962	NR4A3
nsv5909472	copy number variation	1	nstd209	human		GRCh38 chr9: 99,862,498-99,862,580 , GRCh37.p13 chr9: 102,624,780-102,624,862	NR4A3
nsv5723608	mobile element insertion	1	nstd211	human		GRCh38 chr9: 99,850,048-99,850,048 , GRCh37.p13 chr9: 102,612,330-102,612,330	NR4A3
nsv5701806	mobile element insertion	1	nstd211	human		GRCh38 chr9: 99,864,263-99,864,263 , GRCh37.p13 chr9: 102,626,545-102,626,545	NR4A3
nsv5394785	mobile element insertion	1	nstd206	human		GRCh38 chr9: 99,864,263-99,864,314 , GRCh37.p13 chr9: 102,626,545-102,626,596	NR4A3
nsv5381561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807	TBC1D2, ZNF782, 170 more genes
nsv5131924	mobile element insertion	1	nstd203	human		GRCh38 chr9: 99,839,436-99,839,455 , GRCh37.p13 chr9: 102,601,718-102,601,737	NR4A3
nsv4982757	copy number variation	1	nstd200	human		GRCh38 chr9: 99,850,629-99,850,694 , GRCh37.p13 chr9: 102,612,911-102,612,976	NR4A3
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	RPS26P37, MIR27B, 238 more genes
nsv4480572	mobile element insertion	1	nstd166	human		GRCh37.p13 chr9: 102,594,665-102,594,665 , GRCh38.p12 chr9: 99,832,383-99,832,383	NR4A3
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4337085	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042	, ABCA1, 927 more genes
nsv4183881	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 102,580,000-102,585,000 , GRCh38.p12 chr9: 99,817,718-99,822,718	LOC101928438, NR4A3
nsv4175288	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 102,619,824-102,619,940 , GRCh38.p12 chr9: 99,857,542-99,857,658	NR4A3
nsv3922685	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076	MUSK, LOC105376176, 464 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3922633	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312	RAD23B, RNU6-432P, 262 more genes
nsv3922551	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849	HEMGN, LOC105376183, 243 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 147

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 147

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Recent activity