dbVar for Gene (Select 100507346) - 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
nsv5674178	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 98,204,264-98,271,831 , GRCh38.p12 chr9: 95,441,982-95,509,549	LOC100507346, PTCH1
nsv5673897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 98,229,392-98,232,219 , GRCh38.p12 chr9: 95,467,110-95,469,937	PTCH1, LOC100507346
nsv5564503	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 98,226,337-98,248,166 , GRCh38.p12 chr9: 95,464,055-95,485,884	LOC100507346, PTCH1
nsv5381561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807	TBC1D2, ZNF782, 170 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	RPS26P37, MIR27B, 238 more genes
nsv4684056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 98,209,194-98,279,102 , GRCh38.p12 chr9: 95,446,912-95,516,820	PTCH1, LOC100507346
nsv4682878	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 98,209,194-98,270,643 , GRCh38.p12 chr9: 95,446,912-95,508,361	LOC100507346, PTCH1
nsv4681323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 98,209,194-98,279,100 , GRCh38.p12 chr9: 95,446,912-95,516,818	LOC100507346, PTCH1
nsv4676103	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211	MIR3074, LOC112268039, 108 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
nsv4456543	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 98,156,960-99,345,624 , GRCh38.p12 chr9: 95,394,678-96,583,342	LOC105376157, LOC107987103, 26 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
nsv4450326	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,101,697-95,508,371 , GRCh37 chr9: 97,863,979-98,270,653	RNA5SP288, FANCC, 9 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
nsv3963517	copy number variation	1	nstd168	human		GRCh38 chr9: 95,455,744-95,485,309 , GRCh37.p13 chr9: 98,218,026-98,247,591	LOC100507346, PTCH1
nsv3922790	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 94,713,892-98,121,186 , GRCh37 chr9: 97,476,174-100,883,468 , NCBI36 chr9: 96,515,995-99,923,289	CDC14B, PTCH1, 87 more genes
nsv3922685	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076	MUSK, LOC105376176, 464 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
nsv3922615	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 91,596,533-97,018,746 , GRCh37 chr9: 94,358,815-99,781,028 , NCBI36 chr9: 93,398,636-98,820,849	LOC107987097, MIR4670, 137 more genes
nsv3922551	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849	HEMGN, LOC105376183, 243 more genes

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Items: 1 to 20 of 114

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Number of Variants: 20

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