dbVar for Gene (Select 79095) - 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
nsv7071535	inversion	1	nstd229	human		GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289	PTGES2-AS1, STXBP1, 130 more genes
nsv6876756	copy number variation	1	nstd229	human		GRCh38 chr9: 128,152,180-128,158,809 , GRCh37.p13 chr9: 130,914,459-130,921,088	LCN2, BBLN
nsv6868818	copy number variation	1	nstd229	human		GRCh38 chr9: 128,154,721-128,161,088 , GRCh37.p13 chr9: 130,917,000-130,923,367	BBLN
nsv6862466	copy number variation	1	nstd229	human		GRCh38 chr9: 128,160,901-128,161,900 , GRCh37.p13 chr9: 130,923,180-130,924,179	BBLN
nsv6858409	copy number variation	1	nstd229	human		GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979	BBLN, SH2D3C, 47 more genes
nsv6858157	copy number variation	1	nstd229	human		GRCh38 chr9: 128,079,047-128,161,482 , GRCh37.p13 chr9: 130,841,326-130,923,761	BBLN, PTGES2, 4 more genes
nsv6634454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944	HNRNPA1P41, GAS1RR, 1868 more genes
nsv6571772	inversion	1	nstd223	human		GRCh38 chr9: 128,158,123-128,158,936 , GRCh37.p13 chr9: 130,920,402-130,921,215	BBLN
nsv6438804	copy number variation	1	nstd223	human		GRCh38 chr9: 128,155,450-128,158,935 , GRCh37.p13 chr9: 130,917,729-130,921,214	BBLN
nsv6438803	copy number variation	1	nstd223	human		GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679	MIR199B, FPGS, 72 more genes
nsv6314001	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954	LOC105376244, RN7SL187P, 286 more genes
nsv6313546	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937	FAM27C, DPM2, 2166 more genes
nsv6312681	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857	EEIG1, PIP5KL1, 32 more genes
nsv6291261	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529	PTPA, AK1, 123 more genes
nsv6137057	copy number variation	1	nstd213	human		GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614	CRAT, GLE1, 145 more genes
nsv5564479	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714	PIP5KL1, MIR3911, 50 more genes
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
nsv4983738	copy number variation	1	nstd200	human		GRCh38 chr9: 128,155,449-128,158,935 , GRCh37.p13 chr9: 130,917,728-130,921,214	BBLN
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

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Has Clinical Interpretation

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Items: 1 to 20 of 149

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Number of Variants: 20

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