dbVar for Gene (Select 975) - 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
nsv5980257	insertion	1	nstd209	human		GRCh38 chr11: 2,385,603-2,385,603 , GRCh37.p13 chr11: 2,406,833-2,406,833	CD81
nsv5918738	copy number variation	1	nstd209	human		GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188	, TALDO1, 128 more genes
nsv5911945	copy number variation	1	nstd209	human		GRCh38 chr11: 2,385,603-2,385,664 , GRCh37.p13 chr11: 2,406,833-2,406,894	CD81
nsv5662464	insertion	2	nstd207	human		GRCh38 chr11: 2,385,603-2,385,603 , GRCh37.p13 chr11: 2,406,833-2,406,833	CD81
nsv5656213	insertion	1	nstd207	human		GRCh38 chr11: 2,379,452-2,379,452 , GRCh37.p13 chr11: 2,400,682-2,400,682	CD81
nsv5590726	copy number variation	1	nstd207	human		GRCh38 chr11: 2,379,375-2,379,436 , GRCh37.p13 chr11: 2,400,605-2,400,666	CD81
nsv5588096	copy number variation	1	nstd207	human		GRCh38 chr11: 2,385,603-2,385,664 , GRCh37.p13 chr11: 2,406,833-2,406,894	CD81
nsv5512849	copy number variation	1	nstd206	human		GRCh38 chr11: 2,383,591-2,383,642 , GRCh37.p13 chr11: 2,404,821-2,404,872	CD81
nsv5508746	copy number variation	1	nstd206	human		GRCh38 chr11: 2,346,000-2,376,000 , GRCh37.p13 chr11: 2,367,230-2,397,230	CD81, LOC105376520, 1 more genes
nsv5380885	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798	LINC02688, MIR210, 156 more genes
nsv5250662	copy number variation	1	nstd204	human		GRCh37.p13 chr11: 2,329,631-2,409,630 , GRCh38.p13 chr11: 2,308,401-2,388,400	CD81, TSPAN32, 4 more genes
nsv4984139	copy number variation	1	nstd200	human		GRCh38 chr11: 2,323,266-2,387,977 , GRCh37.p13 chr11: 2,344,496-2,409,207	LOC105376520, CD81, 2 more genes
nsv4768373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811	LOC107984302, STK33, 375 more genes
nsv4762151	insertion	1	nstd199	human		GRCh37 chr11: 2,400,676-2,400,676 , GRCh38.p12 chr11: 2,379,446-2,379,446	CD81
nsv4751865	inversion	1	nstd199	human		GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187	, ACP2, 1686 more genes
nsv4749997	copy number variation	1	nstd199	human		GRCh37 chr11: 2,406,860-2,406,922 , GRCh38.p12 chr11: 2,385,630-2,385,692	CD81
nsv4729112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307	OR51E1, TNNI2, 203 more genes
nsv4728784	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 2,316,896-2,418,571 , GRCh38.p12 chr11: 2,295,666-2,397,341	LOC105376520, CD81, 6 more genes
nsv4681827	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755	LOC105376517, KRTAP5-2, 99 more genes
nsv4679705	copy number variation	1	nstd189	human		GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027	, ART1, 50 more genes

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Number of Variants: 20

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dbVar

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Object Type

Organism

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Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 249

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Number of Variants: 20

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