msh6[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
nsv3873570	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,771,371-47,793,044 , NCBI36 chr2: 47,852,014-47,873,687 , GRCh37 chr2: 47,998,510-48,020,183	MSH6
nsv1398093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,007,276-48,020,272 , GRCh38 chr2: 47,780,137-47,793,133	MSH6
nsv1398395	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,783,082-47,791,123 , GRCh37 chr2: 48,010,221-48,018,262	MSH6
nsv3874645	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh38 chr2: 47,783,224-47,791,133 , GRCh37 chr2: 48,010,363-48,018,272	MSH6
nsv3884713	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,367-48,018,268 , GRCh38 chr2: 47,783,228-47,791,129	MSH6
nsv1398165	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,372-48,018,262 , GRCh38 chr2: 47,783,233-47,791,123	MSH6
nsv5564249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,783,232-47,787,317 , GRCh37 chr2: 48,010,371-48,014,456	MSH6
nsv5564334	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,371-48,014,019 , GRCh38 chr2: 47,783,232-47,786,880	MSH6
nsv4682639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,030,549-48,030,834 , GRCh38.p12 chr2: 47,803,410-47,803,695	MSH6
nsv7096513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,010,373-48,010,652 , GRCh38.p12 chr2: 47,783,234-47,783,513	MSH6
nsv3872186	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr2: 48,010,363-48,010,642 , GRCh38 chr2: 47,783,224-47,783,503	MSH6
nsv3883444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,030,553-48,030,830 , GRCh38 chr2: 47,803,414-47,803,691	MSH6
nsv3872690	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,783,228-47,783,499 , GRCh37.p13 chr2: 48,010,367-48,010,638	MSH6
nsv7096172	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,018,046-48,018,282 , GRCh38.p12 chr2: 47,790,907-47,791,143	MSH6
nsv4450168	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,790,917-47,791,133 , GRCh37 chr2: 48,018,056-48,018,272	MSH6
nsv3873129	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,790,927-47,791,123 , GRCh37 chr2: 48,018,066-48,018,262	MSH6
nsv6634491	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,799,804-47,799,882 , GRCh37 chr2: 48,026,943-48,027,021	MSH6
nsv3878435	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 48,030,765-48,030,829 , GRCh38 chr2: 47,803,626-47,803,690	MSH6
nsv4681490	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr2: 48,010,373-48,018,272 , GRCh38.p12 chr2: 47,783,234-47,791,133	MSH6
nsv4682544	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr2: 48,010,373-48,010,642 , GRCh38.p12 chr2: 47,783,234-47,783,503	MSH6

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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 141

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Number of Variants: 20

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