"nstd102"[study] AND "lynch"[Clinical Phenotype] AND "syndrome"[Clinic - 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
nsv3874987	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,403,067-47,483,228 , GRCh37 chr2: 47,630,206-47,710,367	MSH2
nsv1397982	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,403,124-47,480,871 , GRCh37 chr2: 47,630,263-47,708,010	MSH2
nsv3886121	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,639,553-47,710,367 , GRCh38 chr2: 47,412,414-47,483,228	MSH2
nsv1398467	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,639,553-47,710,360 , GRCh38 chr2: 47,412,414-47,483,221	MSH2
nsv3877028	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,641,408-47,710,088 , GRCh38.p12 chr2: 47,414,269-47,482,949	MSH2
nsv1398427	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,403,124-47,471,062 , GRCh37 chr2: 47,630,263-47,698,201	MSH2
nsv1397940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,630,263-47,693,947 , GRCh38 chr2: 47,403,124-47,466,808	MSH2
nsv1397932	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,429,742-47,483,221 , GRCh37 chr2: 47,656,881-47,710,360	MSH2
nsv4685914	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr2: 47,657,081-47,709,917 , GRCh38.p12 chr2: 47,429,942-47,482,778	MSH2
nsv1398247	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,403,124-47,445,657 , GRCh37 chr2: 47,630,263-47,672,796	MSH2
nsv4685890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,657,081-47,698,103 , GRCh38.p12 chr2: 47,429,942-47,470,964	MSH2
nsv1398423	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,672,687-47,710,360 , GRCh38 chr2: 47,445,548-47,483,221	MSH2
nsv1398548	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,632,107-47,668,733 , GRCh38 chr2: 47,404,968-47,441,594	MSH2
nsv3874725	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 47,445,548-47,480,871 , GRCh37.p13 chr2: 47,672,687-47,708,010	MSH2
nsv6634316	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 47,618,487-47,650,860 , GRCh38.p12 chr2: 47,391,348-47,423,721	MSH2
nsv3876211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,641,519-47,672,796 , GRCh38.p12 chr2: 47,414,380-47,445,657	MSH2
nsv1398585	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 6,012,870-6,042,267 , GRCh38 chr7: 5,973,239-6,002,636	PMS2
nsv1398480	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 47,630,263-47,657,080 , GRCh38 chr2: 47,403,124-47,429,941	MSH2
nsv6636035	copy number variation	3	nstd102	human	Pathogenic	GRCh38 chr2: 47,403,067-47,429,741 , GRCh37 chr2: 47,630,206-47,656,880	MSH2
nsv4685960	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 47,630,542-47,656,880 , GRCh38.p12 chr2: 47,403,403-47,429,741	MSH2

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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

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Items: 1 to 20 of 279

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Number of Variants: 20

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