mtmr1[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
nsv3872352	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 149,917,987-149,931,106 , GRCh38.p12 chrX: 150,749,515-150,762,633	MTMR1
nsv3876870	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 149,913,184-149,933,341 , GRCh38.p12 chrX: 150,744,712-150,764,868	MTMR1, CD99L2
nsv3883995	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,535,674-149,896,019 , GRCh38.p12 chrX: 150,367,407-150,727,547	MTMR1, MTM1, 2 more genes
nsv3896695	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 150,449,408-150,750,615 , GRCh37 chrX: 149,617,674-149,782,550 , NCBI36 chrX: 149,368,332-149,669,745	MTMR1, MAMLD1, 2 more genes
nsv4728353	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,747,506-150,037,141 , GRCh38.p12 chrX: 150,579,046-150,868,668	MTMR1, CYP2C64P, 3 more genes
nsv4728150	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,702,307-149,971,697 , GRCh38.p12 chrX: 150,533,858-150,803,224	MTMR1, CD99L2, 2 more genes
nsv3901905	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,742,664-150,007,069 , NCBI36 chrX: 149,493,322-149,757,727 , GRCh38 chrX: 150,574,214-150,838,596	MTMR1, CYP2C64P, 3 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	MTMR1, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	MTMR1, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	MTMR1, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	MTMR1, H2AB2, 2152 more genes
nsv3898149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792	MTMR1, OR3B1P, 2154 more genes
nsv3877395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174	MTMR1, ARMCX2, 2154 more genes
nsv3884935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127	MTMR1, NDUFB11, 2154 more genes
nsv3903061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832	MTMR1, SLC38A5, 2152 more genes
nsv3885865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920	MTMR1, MIR1277, 2152 more genes
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	MTMR1, LOC105373176, 2151 more genes
nsv3907545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293	MTMR1, TMEM30BP1, 2151 more genes
nsv3884029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101	MTMR1, SSX4B, 2150 more genes
nsv3898185	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431	MTMR1, ANKRD11P2, 2151 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 191

Page of 10

Number of Variants: 20

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Supplemental Content

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