dbVar for Gene (Select 100420501) - 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
nsv5473938	copy number variation	1	nstd206	human		GRCh38 chr9: 94,280,000-94,576,600 , GRCh37.p13 chr9: 97,042,282-97,338,882	LOC107987023, PCAT7, 12 more genes
nsv5185749	mobile element insertion	1	nstd203	human		GRCh38 chr9: 94,433,697-94,433,706 , GRCh37.p13 chr9: 97,195,979-97,195,988	MFSD14B, YRDCP1
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
nsv4684026	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 96,160,235-97,428,496 , GRCh38.p12 chr9: 93,397,953-94,666,214	FBP1, PHF2, 30 more genes
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
nsv4607418	copy number variation	1	nstd183	human		GRCh37 chr9: 96,999,239-97,239,821 , GRCh38.p12 chr9: 94,236,957-94,477,539	VDAC1P11, ZNF169, 8 more genes
nsv4526567	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 97,194,999-97,543,000 , GRCh38.p12 chr9: 94,432,717-94,780,718	LOC107987101, FBP2, 8 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
nsv4415153	copy number variation	1	nstd174	human		GRCh37 chr9: 96,999,227-97,356,950 , GRCh38.p12 chr9: 94,236,945-94,594,668	FBP2, NUTM2F, 13 more genes
nsv4368771	copy number variation	1	nstd173	human		GRCh37 chr9: 97,179,187-97,334,924 , GRCh38.p12 chr9: 94,416,905-94,572,642	FBP2, MFSD14B, 5 more genes
nsv4349215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992	SPATA31C1, LINC02893, 280 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
nsv4178746	copy number variation	1	nstd166	human		GRCh37.p13 chr9: 97,180,000-97,199,000 , GRCh38.p12 chr9: 94,417,718-94,436,718	YRDCP1, MFSD14B
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
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

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Number of Variants: 20

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