dbVar for Gene (Select 51117) - 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
nsv5923980	copy number variation	1	nstd209	human		GRCh38 chr9: 128,326,706-128,327,010 , GRCh37.p13 chr9: 131,088,985-131,089,289	COQ4
nsv5488330	copy number variation	1	nstd206	human		GRCh38 chr9: 128,326,731-128,326,997 , GRCh37.p13 chr9: 131,089,010-131,089,276	COQ4
nsv5484049	copy number variation	1	nstd206	human		GRCh38 chr9: 128,329,682-128,329,802 , GRCh37.p13 chr9: 131,091,961-131,092,081	COQ4
nsv4985740	copy number variation	1	nstd200	human		GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573	, SET, 33 more genes
nsv4768374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685	COQ4, GLE1, 53 more genes
nsv4683557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,577,951-131,303,459 , GRCh38.p12 chr9: 127,815,672-128,541,180	SWI5, LOC105379841, 36 more genes
nsv4675731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931	PTPA, GLE1, 55 more genes
nsv4675555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,094,304-131,863,858 , GRCh38.p12 chr9: 128,332,025-129,101,579	ENDOG, SPOUT1, 35 more genes
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
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
nsv4450425	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997	RNU7-171P, MIR2861, 50 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
nsv4186929	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 131,089,010-131,089,276 , GRCh38.p12 chr9: 128,326,731-128,326,997	COQ4
nsv3924593	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 130,038,447-130,714,167 , GRCh38 chr9: 128,236,347-128,912,067 , GRCh37 chr9: 130,998,626-131,674,346	LRRC8A, SPOUT1, 34 more genes
nsv3924370	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225	MVB12B, MIR4672, 97 more genes
nsv3923672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,681,755-132,842,253 , GRCh38 chr9: 127,919,476-130,079,974 , NCBI36 chr9: 129,721,576-131,882,074	PIP5KL1, NTMT1, 80 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

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Has Clinical Interpretation

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Items: 1 to 20 of 129

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Number of Variants: 20

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