tmem177[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3884947	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 120,361,528-120,438,756 , GRCh38.p12 chr2: 119,603,952-119,681,180	TMEM177, CFAP221
nsv3923683	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 120,102,942-120,243,758 , GRCh37.p13 chr2: 120,386,472-120,527,288 , GRCh38.p12 chr2: 119,628,896-119,769,712	TMEM177, RPL17P15, 3 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	TMEM177, DAZAP2P1, 2991 more genes
nsv3894414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 118,843,900-135,722,308 , GRCh38 chr2: 118,086,324-134,964,738 , NCBI36 chr2: 118,560,370-135,438,778	TMEM177, RHOQP2, 287 more genes
nsv3873957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 109,798,247-125,658,380 , GRCh38.p12 chr2: 109,181,791-124,900,803	TMEM177, MTND1P28, 230 more genes
nsv6313770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124	TMEM177, LOC105373575, 174 more genes
nsv3892279	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 115,776,113-129,545,173 , GRCh37 chr2: 116,059,643-129,828,703 , GRCh38 chr2: 115,302,067-129,071,130	TMEM177, MAP3K2, 144 more genes
nsv3921001	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 115,444,912-126,178,935 , GRCh37.p13 chr2: 115,728,442-126,462,465 , GRCh38.p12 chr2: 114,970,865-125,704,888	TMEM177, RPL27P7, 94 more genes
nsv3889486	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 114,707,932-124,328,692 , GRCh38.p12 chr2: 113,950,355-123,571,116	TMEM177, LOC107985817, 91 more genes
nsv3873783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 114,056,441-123,673,800 , GRCh38.p12 chr2: 113,298,864-122,916,224	TMEM177, INHBB, 111 more genes
nsv3880973	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 117,070,953-126,303,416 , GRCh38.p12 chr2: 116,313,377-125,545,839	TMEM177, LOC105373585, 86 more genes
nsv4674710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 118,872,395-128,069,813 , GRCh38.p12 chr2: 118,114,819-127,312,237	TMEM177, C2orf76, 89 more genes
nsv3879351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 116,754,600-123,897,370 , GRCh38.p12 chr2: 115,997,024-123,139,794	TMEM177, LOC107985815, 78 more genes
nsv6636871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686	TMEM177, LOC105373578, 78 more genes
nsv4674062	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 115,416,190-122,399,064 , GRCh38.p12 chr2: 114,658,613-121,641,488	TMEM177, DPP10-AS3, 71 more genes
nsv4674739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 118,903,294-123,099,547 , GRCh38.p12 chr2: 118,145,718-122,341,971	TMEM177, LOC101927709, 55 more genes
nsv3895925	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 119,161,875-122,095,860 , GRCh37 chr2: 119,445,405-122,379,390 , GRCh38 chr2: 118,687,829-121,621,814	TMEM177, GLI2, 41 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	TMEM177, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	TMEM177, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	TMEM177, RNU6-674P, 3735 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:

Search results

Items: 1 to 20 of 28

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 28

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity