MTM1 - 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
nsv4452921	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,761,067-149,840,078 , GRCh38.p12 chrX: 150,592,605-150,671,605	MTM1
nsv4683823	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,751,687-149,817,005 , GRCh38.p12 chrX: 150,583,227-150,648,532	MTM1
nsv7137088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,761,077-149,818,374 , GRCh38.p12 chrX: 150,592,615-150,649,901	MTM1
nsv7148259	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 150,592,508-150,619,237 , GRCh37.p13 chrX\|NW_004070890.2: 6,116,906-6,143,635 , GRCh37.p13 chrX: 149,760,970-149,787,710	MTM1
nsv3919421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,826,274-149,840,088 , GRCh38.p12 chrX: 150,657,801-150,671,615	MTM1
nsv4454861	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,831,886-149,840,088 , GRCh38.p12 chrX: 150,663,413-150,671,615	MTM1
nsv4681979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,831,896-149,832,092 , GRCh38.p12 chrX: 150,663,423-150,663,619	MTM1
nsv6313318	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 149,761,067-149,761,149 , GRCh38.p12 chrX: 150,592,605-150,592,687	MTM1
nsv7098996	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 150,568,597-150,568,662 , GRCh37 chrX: 149,737,047-149,737,112	MTM1
nsv997162	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 149,737,047-149,841,616 , GRCh38.p12 chrX: 150,568,597-150,673,143	MTM1
nsv7097993	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 149,761,093-149,767,213 , GRCh38.p12 chrX: 150,592,631-150,598,749	MTM1
nsv4452642	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 149,783,042-149,787,632 , GRCh38.p12 chrX: 150,614,569-150,619,159	MTM1
nsv3913475	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 149,826,274-149,826,520 , GRCh38.p12 chrX: 150,657,801-150,658,047	MTM1
nsv7097994	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 149,818,176-149,818,384 , GRCh38.p12 chrX: 150,649,703-150,649,911	MTM1
nsv3910009	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 149,826,294-149,826,500 , GRCh38.p12 chrX: 150,657,821-150,658,027	MTM1
nsv4683150	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,839,891-149,840,078 , GRCh38.p12 chrX: 150,671,418-150,671,605	MTM1
nsv4682507	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,783,052-149,840,078 , GRCh38.p12 chrX: 150,614,579-150,671,605	MTM1
nsv7098594	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,761,077-149,787,632 , GRCh38.p12 chrX: 150,592,615-150,619,159	MTM1
nsv3879535	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,818,189-149,840,068 , GRCh38.p12 chrX: 150,649,716-150,671,595	MTM1
nsv6313319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 149,807,406-149,814,354 , GRCh38.p12 chrX: 150,638,933-150,645,881	MTM1

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 446

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Number of Variants: 20

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