cga[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
nsv4675382	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 87,724,126-87,800,047 , GRCh38.p12 chr6: 87,014,408-87,090,329	CGA, HTR1E, 1 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	CGA, LOC107986534, 426 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	CGA, SPACA1, 187 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	CGA, RNU4-72P, 157 more genes
nsv3893892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,783,137-96,908,198 , GRCh38.p12 chr14: 84,316,793-96,441,861	DICER1, SERPINA13P, 175 more genes
nsv4675107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153	SHLD2P2, RPL15P2, 175 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	CGA, ME1, 136 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	CGA, LOC105377882, 117 more genes
nsv3918084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697	CGA, LOC105377897, 91 more genes
nsv6314190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555	EML5, LOC105370612, 104 more genes
nsv7137135	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555	LOC100128939, FAM181A-AS1, 104 more genes
nsv3912992	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512	CGA, DNAJC19P6, 88 more genes
nsv3922566	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786	RPSAP4, LOC105370622, 97 more genes
nsv6290989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748	CGA, KRT18P30, 58 more genes
nsv4675039	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994	CGA, C6orf163, 65 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	CGA, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	CGA, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	CGA, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	CGA, ITPR3, 2905 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	LOC440181, HEATR5A-DT, 1998 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 57

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Number of Variants: 20

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