cd82[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
nsv4675915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 44,568,649-44,842,619 , GRCh38.p12 chr11: 44,547,099-44,821,068	CD82, TSPAN18, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CD82, FAUP4, 2031 more genes
nsv3922177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947	CD82, MIR3160-2, 122 more genes
nsv3913842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735	CD82, MIR3160-1, 162 more genes
nsv3924778	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131	CD82, F2, 140 more genes
nsv6291196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167	CD82, LINC02687, 86 more genes
nsv3917236	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,706,376-44,866,811 , GRCh38 chr11: 39,684,826-44,845,260 , NCBI36 chr11: 39,662,952-44,823,387	CD82, LOC107984328, 42 more genes
nsv3921841	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 42,531,785-46,092,919 , GRCh37 chr11: 42,575,209-46,136,343 , GRCh38 chr11: 42,553,659-46,114,792	CD82, PEX16, 51 more genes
nsv3919271	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 44,136,593-46,121,139 , NCBI36 chr11: 44,114,719-46,099,266 , GRCh37 chr11: 44,158,143-46,142,690	CD82, LOC105376646, 31 more genes
nsv3893813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,769,206-44,958,891 , GRCh38.p12 chr11: 43,747,656-44,937,340	CD82, ACCSL, 16 more genes
nsv6315539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,769,957-44,952,669 , GRCh38.p12 chr11: 43,748,407-44,931,118	CD82, ACCS, 16 more genes
nsv997191	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr11: 43,894,800-46,152,450 , GRCh38.p12 chr11: 43,873,250-46,130,899	CD82, CRY2, 39 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	CD82, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	CD82, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	CD82, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	CD82, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	CD82, TRR-TCT3-2, 494 more genes
nsv3914563	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735	CD82, ACP2, 143 more genes
nsv4675520	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 44,502,129-44,788,186 , GRCh38.p12 chr11: 44,480,579-44,766,636	CD82, LOC105376646, 4 more genes
nsv3921625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 40,710,224-44,934,960 , NCBI36 chr11: 40,666,800-44,891,536 , GRCh38 chr11: 40,688,674-44,913,409	CD82, CTBP2P6, 36 more genes

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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 23

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Number of Variants: 20

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Supplemental Content

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Search details

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