dbVar for Gene (Select 50833) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7039806	inversion	1	nstd229	human		GRCh38 chr7: 122,936,203-123,057,960 , GRCh37.p13 chr7: 122,576,257-122,698,014	LOC105375482, TAS2R16
nsv6828878	copy number variation	1	nstd229	human		GRCh38 chr7: 122,988,954-123,005,778 , GRCh37.p13 chr7: 122,629,008-122,645,832	TAS2R16
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	RRBP1P1, SLC29A4P1, 2680 more genes
nsv6615286	copy number variation	1	nstd223	human		GRCh38 chr7: 122,942,257-123,142,187 , GRCh37.p13 chr7: 122,582,311-122,782,241	SLC13A1, LOC105375482, 1 more genes
nsv6603026	copy number variation	1	nstd223	human		GRCh38 chr7: 122,721,599-123,353,768 , GRCh37.p13 chr7: 122,361,653-122,993,822	SLC13A1, TAS2R16, 4 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	AOC1, ACHE, 2682 more genes
nsv6314995	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575	CAPZA2, CAV1, 109 more genes
nsv6313851	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648	DOCK4-AS1, RPL3P8, 262 more genes
nsv6136546	copy number variation	1	nstd213	human		GRCh37 chr7: 120,110,000-126,120,001 , GRCh38.p12 chr7: 120,469,946-126,479,947	SSU72L6, IQUB, 67 more genes
nsv6135872	copy number variation	1	nstd213	human		GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947	CAV1, SLC13A1, 154 more genes
nsv6135545	copy number variation	1	nstd213	human		GRCh37 chr7: 117,870,000-125,940,001 , GRCh38.p12 chr7: 118,229,946-126,299,947	GPR37, KCND2, 78 more genes
nsv5556846	sequence alteration	1	nstd206	human		GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670	, AHR, 2675 more genes
nsv5381759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640	TMEM229A, ST7-OT3, 110 more genes
nsv5326600	inversion	1	nstd204	human		GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904	, ARF5, 752 more genes
nsv5039775	inversion	1	nstd200	human		GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114	, NFE4, 1832 more genes
nsv5029742	inversion	1	nstd200	human		GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680	, LOC100533722, 1168 more genes
nsv4968685	copy number variation	1	nstd200	human		GRCh38 chr7: 122,962,765-123,007,106 , GRCh37.p13 chr7: 122,602,819-122,647,160	TAS2R16, LOC105375482
nsv4968684	copy number variation	1	nstd200	human		GRCh38 chr7: 122,942,257-123,142,187 , GRCh37.p13 chr7: 122,582,311-122,782,241	SLC13A1, LOC105375482, 1 more genes
nsv4880762	inversion	1	nstd200	human		GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588	, RN7SKP277, 1168 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	RPL26P23, ST13P17, 887 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 119

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 119

Page of 6

Number of Variants: 20

Page of 6

Supplemental Content

Find related data

Recent activity