selenos[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
nsv3924161	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 101,678,725-101,833,366 , GRCh38 chr15: 101,138,520-101,293,161	SELENOS, CHSY1, 3 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	SELENOS, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	SELENOS, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	SELENOS, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	SELENOS, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	SELENOS, RPL31P55, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	SELENOS, SNRPCP18, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	SELENOS, LOC105371009, 149 more genes
nsv3919064	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 91,542,950-100,200,996 , GRCh38 chr15: 93,198,717-101,843,270 , GRCh37 chr15: 93,741,946-102,383,473	SELENOS, LOC105371032, 126 more genes
nsv3918825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,348,261-101,867,081 , GRCh38 chr15: 93,805,032-101,326,876 , NCBI36 chr15: 92,149,265-99,684,604	SELENOS, LOC440311, 107 more genes
nsv3922914	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189	SELENOS, OR4F14P, 124 more genes
nsv3897684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 95,136,822-102,045,577 , GRCh38.p12 chr15: 94,593,593-101,505,374	SELENOS, ARRDC4, 98 more genes
nsv3921313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,313,856-102,351,195 , NCBI36 chr15: 94,114,860-100,168,718 , GRCh38 chr15: 95,770,627-101,810,992	SELENOS, SPATA8-AS1, 97 more genes
nsv3923265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,567,356-102,461,201 , NCBI36 chr15: 94,368,360-100,278,724 , GRCh38 chr15: 96,024,127-101,920,998	SELENOS, LOC107987228, 104 more genes
nsv3911877	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 94,413,658-100,207,304 , GRCh38 chr15: 96,069,425-101,849,578 , GRCh37 chr15: 96,612,654-102,389,781	SELENOS, LOC400464, 99 more genes
nsv4578637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,878,099-102,397,836 , GRCh38.p12 chr15: 96,334,870-101,857,633	SELENOS, SYNM-AS1, 94 more genes
nsv3918683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 96,329,791-101,849,578 , NCBI36 chr15: 94,674,024-100,207,304 , GRCh37 chr15: 96,873,020-102,389,781	SELENOS, LYSMD4, 95 more genes
nsv4350607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,873,212-102,389,423 , GRCh38.p12 chr15: 96,329,983-101,849,220	SELENOS, LOC105371010, 95 more genes
nsv3891450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 96,913,435-102,429,112 , GRCh38.p12 chr15: 96,370,206-101,888,909	SELENOS, LOC107984790, 96 more genes
nsv6314152	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 97,026,327-102,429,112 , GRCh38.p12 chr15: 96,483,097-101,888,909	SELENOS, PCSK6, 92 more genes

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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 102

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Number of Variants: 20

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