ndufa7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4683116	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 8,367,327-8,373,194 , GRCh38.p12 chr19: 8,302,443-8,308,310	NDUFA7, CD320
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	NDUFA7, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	NDUFA7, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	NDUFA7, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	NDUFA7, SEMA6B, 299 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	NDUFA7, PCP2, 250 more genes
nsv3888397	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059	NDUFA7, ELAVL1, 80 more genes
nsv3922045	copy number variation	1	nstd102	human	Benign	NCBI36 chr19: 8,049,599-8,279,452 , GRCh37 chr19: 8,143,599-8,373,452 , GRCh38 chr19: 8,078,715-8,308,568	NDUFA7, CERS4, 4 more genes
nsv7095676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710	NDUFA7, LRRC8E, 53 more genes
nsv4676269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878	NDUFA7, LRRC8E, 47 more genes
nsv4682037	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310	NDUFA7, XAB2, 40 more genes
nsv3921240	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 8,025,412-8,572,615 , GRCh37.p13 chr19: 8,119,412-8,666,615 , GRCh38.p12 chr19: 8,054,528-8,601,731	NDUFA7, ADAMTS10, 18 more genes

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ndufa7[All Fields] AND 1[has_clinical] (13)
dbVar
Homo sapiens clone MGC:15139 IMAGE:4302390
Homo sapiens clone MGC:15139 IMAGE:4302390
gi|14250827|gb|BC008884.1|BC008884

Nucleotide
The epidemiology of EBV and its association with malignant disease - Human Herpe...
The epidemiology of EBV and its association with malignant disease - Human Herpesviruses

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