tmem123[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
nsv3901064	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 102,298,002-102,306,750 , GRCh38.p12 chr11: 102,427,271-102,436,019	TMEM123
nsv3903081	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 102,300,876-102,306,750 , GRCh38.p12 chr11: 102,430,145-102,436,019	TMEM123
nsv3893849	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 102,300,876-102,306,515 , GRCh38.p12 chr11: 102,430,145-102,435,784	TMEM123
nsv3897486	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 102,300,876-102,306,430 , GRCh38.p12 chr11: 102,430,145-102,435,699	TMEM123
nsv3905047	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 102,305,304-102,306,750 , GRCh38.p12 chr11: 102,434,573-102,436,019	TMEM123
nsv3899504	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 102,249,285-102,323,664 , GRCh38.p12 chr11: 102,378,554-102,452,933	TMEM123, BIRC2, 1 more genes
nsv3898420	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 102,323,664-102,401,448 , GRCh38.p12 chr11: 102,452,933-102,530,717	TMEM123, MMP7, 2 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 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	TMEM123, FAUP4, 2031 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	EIF2S2P3, CYP17A1-AS1, 895 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	TMEM123, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	TMEM123, PLS1P1, 349 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	TMEM123, PHB1P16, 385 more genes
nsv6637396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313	TMEM123, LOC107984375, 295 more genes
nsv3894488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924	TMEM123, RNU6-16P, 270 more genes
nsv3910663	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308	TMEM123, LOC101060084, 230 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	TMEM123, AMOTL1, 240 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	TMEM123, HSPD1P13, 239 more genes
nsv6637687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793	TMEM123, GRIA4, 111 more genes
nsv3924464	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873	TMEM123, ARHGAP42, 91 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 52

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Number of Variants: 20

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