dbVar for Gene (Select 253039) - 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
nsv5861230	copy number variation	1	nstd209	human		GRCh38 chr9: 120,850,820-120,852,919 , GRCh37.p13 chr9: 123,613,098-123,615,197	CUTALP
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
nsv4830416	copy number variation	1	nstd200	human		GRCh37 chr9: 123,596,208-123,617,768 , GRCh38.p12 chr9: 120,833,930-120,855,490	PHF19, PSMD5, 1 more genes
nsv4481010	mobile element insertion	1	nstd166	human		GRCh37.p13 chr9: 123,608,930-123,608,930 , GRCh38.p12 chr9: 120,846,652-120,846,652	CUTALP
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
nsv4343265	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 123,579,171-124,453,597 , GRCh38.p12 chr9: 120,816,893-121,691,318	C5, GSN, 17 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
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
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
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
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ALOX15P2, LOC107987061, 2184 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	RORB-AS1, FNBP1, 2168 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	OR2AM1P, RN7SL565P, 2174 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	MIR219A2, CLCN3P1, 2183 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	BANCR, SETX, 2173 more genes

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 87

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Number of Variants: 20

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