med17[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
nsv4683928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,517,670-93,545,240 , GRCh38.p12 chr11: 93,784,504-93,812,074	MED17
nsv6309389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,529,711-93,539,976 , GRCh38.p12 chr11: 93,796,545-93,806,810	MED17
nsv5672785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,529,566-93,535,148 , GRCh38.p12 chr11: 93,796,400-93,801,982	MED17
nsv4451419	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 93,784,504-93,788,177 , GRCh37 chr11: 93,517,670-93,521,343	MED17
nsv6309240	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,517,670-93,517,939 , GRCh38.p12 chr11: 93,784,504-93,784,773	MED17
nsv5672639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,521,157-93,521,343 , GRCh38.p12 chr11: 93,787,991-93,788,177	MED17
nsv6309388	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 93,529,566-93,545,240 , GRCh38.p12 chr11: 93,796,400-93,812,074	MED17
nsv6309454	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 93,540,674-93,543,052 , GRCh38.p12 chr11: 93,807,508-93,809,886	MED17
nsv6291002	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 93,468,349-93,587,129 , GRCh38.p12 chr11: 93,735,183-93,853,963	MED17, VSTM5, 3 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	MED17, FAUP4, 2031 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	MED17, 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	MED17, 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	MED17, 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	MED17, LOC107984375, 295 more genes
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	MED17, LOC105369441, 296 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	MED17, RNU6-16P, 270 more genes
nsv6313961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717	MED17, MTND5P38, 252 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	MED17, 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	MED17, AMOTL1, 240 more genes
nsv3897292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057	MED17, FAM181B, 218 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 32

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Number of Variants: 20

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