dbVar for Gene (Select 106479332) - 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
nsv7063188	inversion	1	nstd229	human		GRCh38 chr9: 124,594,053-124,609,017 , GRCh37.p13 chr9: 127,356,332-127,371,296	NR6A1, RN7SL302P, 1 more genes
nsv6637981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289	PBX3-DT, ADGRD2, 119 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
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
nsv6137443	copy number variation	1	nstd213	human		GRCh37 chr9: 126,390,000-129,240,001 , GRCh38.p12 chr9: 123,627,721-126,477,722	NR6A1, GOLGA1, 52 more genes
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
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
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
nsv3922263	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 124,897,698-128,495,943 , GRCh38 chr9: 123,095,598-126,693,843 , GRCh37 chr9: 125,857,877-129,456,122	OLFML2A, LHX2-AS1, 64 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
nsv3919948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805	LOC107987143, ATP6V1G1P3, 456 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
nsv3918439	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,073,102-138,179,445 , GRCh37 chr9: 123,835,380-141,073,897 , NCBI36 chr9: 122,875,201-140,193,718	MIR4478, ENTR1, 498 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

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 78

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Number of Variants: 20

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