dbVar for Gene (Select 10773) - 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
nsv5970603	inversion	1	nstd209	human		GRCh38 chr9: 122,761,784-123,114,887 , GRCh37.p13 chr9: 125,524,063-125,877,166	GPR21, PDCL, 16 more genes
nsv5040732	inversion	1	nstd200	human		GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990	, LOC105379839, 440 more genes
nsv4675789	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 124,604,592-126,306,080 , GRCh38.p12 chr9: 121,842,313-123,543,801	MIR7150, OR1N2, 43 more genes
nsv4612968	copy number variation	1	nstd183	human		GRCh37 chr9: 125,670,505-125,673,088 , GRCh38.p12 chr9: 122,908,226-122,910,809	ZBTB6
nsv4605033	copy number variation	1	nstd183	human		GRCh37 chr9: 125,670,505-125,670,854 , GRCh38.p12 chr9: 122,908,226-122,908,575	ZBTB6
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4457071	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 125,349,988-126,462,569 , GRCh38.p12 chr9: 122,587,709-123,700,290	LOC105376265, OR1L1, 30 more genes
nsv4456842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 125,635,604-125,892,381 , GRCh38.p12 chr9: 122,873,325-123,130,102	LOC100422501, RNY1P15, 11 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4337085	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042	, ABCA1, 927 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3920829	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497	LOC101928786, NRON, 495 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3919948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805	LOC107987143, ATP6V1G1P3, 456 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes
nsv3918439	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,073,102-138,179,445 , GRCh37 chr9: 123,835,380-141,073,897 , NCBI36 chr9: 122,875,201-140,193,718	MIR4478, ENTR1, 498 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	RN7SKP87, SPATA6L, 2168 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 more genes
nsv3915923	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 121,684,719-140,132,214 , GRCh37.p13 chr9: 122,644,898-141,012,393 , GRCh38.p12 chr9: 119,882,620-138,117,941	NRARP, HMGA1P4, 511 more genes

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Number of Variants: 20

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