mtmr12[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
nsv3875724	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,544-32,321,077 , GRCh38.p12 chr5: 32,312,438-32,320,971	MTMR12
nsv3872653	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,505-32,313,087 , GRCh38.p12 chr5: 32,312,399-32,312,981	MTMR12
nsv3877131	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,505-32,313,032 , GRCh38.p12 chr5: 32,312,399-32,312,926	MTMR12
nsv3884603	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,544-32,326,234 , GRCh38.p12 chr5: 32,312,438-32,326,128	MTMR12
nsv3872659	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,658-32,321,077 , GRCh38.p12 chr5: 32,312,552-32,320,971	MTMR12
nsv3873121	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,607-32,317,439 , GRCh38.p12 chr5: 32,312,501-32,317,333	MTMR12
nsv3878470	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 32,312,658-32,317,439 , GRCh38.p12 chr5: 32,312,552-32,317,333	MTMR12
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	MTMR12, MEGF10, 2080 more genes
nsv3914649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397	MTMR12, LOC105374666, 399 more genes
nsv3887142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091	MTMR12, H3Y1, 381 more genes
nsv3910712	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394	MTMR12, ROPN1L, 378 more genes
nsv3924496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010	MTMR12, LOC105374678, 356 more genes
nsv3914100	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 30,184,899-35,249,537 , GRCh38 chr5: 30,149,035-35,213,678 , GRCh37 chr5: 30,149,142-35,213,780	MTMR12, GUSBP18, 61 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	MTMR12, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	MTMR12, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	MTMR12, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	MTMR12, LINC02241, 878 more genes
nsv3923992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984	MTMR12, LOC100130748, 533 more genes
nsv3911295	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861	MTMR12, PMCHL1, 532 more genes
nsv3922539	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845	MTMR12, MTCYBP37, 398 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 36

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Number of Variants: 20

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Supplemental Content

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