tmem175[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3871570	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,035-1,019,312 , GRCh38.p12 chr4: 953,247-1,025,524	TMEM175, SLC26A1, 3 more genes
nsv3876082	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,024-1,019,101 , GRCh38.p12 chr4: 953,236-1,025,313	TMEM175, IDUA, 3 more genes
nsv3882732	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,035-1,019,101 , GRCh38.p12 chr4: 953,247-1,025,313	TMEM175, SLC26A1, 3 more genes
nsv3922676	copy number variation	1	nstd102	human	Benign/Likely benign	NCBI36 chr4: 942,406-1,010,417 , GRCh38 chr4: 958,618-1,026,629 , GRCh37 chr4: 952,406-1,020,417	TMEM175, FGFRL1, 3 more genes
nsv3918564	copy number variation	1	nstd102	human	Benign	NCBI36 chr4: 942,465-1,010,417 , GRCh37 chr4: 952,465-1,020,417 , GRCh38 chr4: 958,677-1,026,629	TMEM175, DGKQ, 3 more genes
nsv4452528	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 850,700-965,829 , GRCh38.p12 chr4: 856,912-972,041	TMEM175, DGKQ, 2 more genes
nsv3885762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123	TMEM175, CD38, 456 more genes
nsv3923296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931	TMEM175, OR7E99P, 446 more genes
nsv4674378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859	TMEM175, USP17L30, 394 more genes
nsv6315347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952	TMEM175, LOC100421802, 375 more genes
nsv6291097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544	TMEM175, LOC105374479, 372 more genes
nsv3915161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608	TMEM175, CTBP1-AS, 370 more genes
nsv1398080	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559	TMEM175, RPL10AP7, 366 more genes
nsv6112747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372	TMEM175, GPR78, 362 more genes
nsv3915014	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 75,040-17,097,463 , GRCh38 chr4: 85,149-17,486,742 , GRCh37 chr4: 85,040-17,488,365	TMEM175, LOC100422637, 350 more genes
nsv3915275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,447-17,279,636 , GRCh38 chr4: 72,555-17,278,013 , NCBI36 chr4: 62,447-16,888,734	TMEM175, OR7E99P, 347 more genes
nsv3888069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760	TMEM175, RPS3AP16, 332 more genes
nsv3917860	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 37,335-15,869,056 , NCBI36 chr4: 27,336-15,479,777 , GRCh37 chr4: 37,336-15,870,679	TMEM175, LOC105374338, 330 more genes
nsv3918310	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-15,658,035 , GRCh37 chr4: 72,447-15,659,658 , NCBI36 chr4: 62,447-15,268,756	TMEM175, RN7SL589P, 323 more genes
nsv3887204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-15,302,739 , GRCh38.p12 chr4: 71,660-15,301,115	TMEM175, USP17L21, 318 more genes

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Number of Variants: 20

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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 157

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Number of Variants: 20

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