dbVar for Gene (Select 641373) - 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
nsv5304644	copy number variation	1	nstd204	human		GRCh37.p13 chr9: 129,166,789-129,173,244 , GRCh38.p13 chr9: 126,404,510-126,410,965	MVB12B, NRON
nsv5248241	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 126,404,404-126,410,978 , GRCh37.p13 chr9: 129,166,683-129,173,257	MVB12B, NRON
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
nsv4985720	copy number variation	1	nstd200	human		GRCh38 chr9: 126,340,928-126,609,468 , GRCh37.p13 chr9: 129,103,207-129,371,747	LOC105376276, LMX1B-DT, 2 more genes
nsv4841798	copy number variation	1	nstd200	human		GRCh37 chr9: 129,103,207-129,371,747 , GRCh38.p12 chr9: 126,340,928-126,609,468	LOC105376276, LMX1B-DT, 2 more genes
nsv4768372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293	LOC105379841, PTRH1, 47 more genes
nsv4676021	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 129,137,576-129,384,914 , GRCh38.p12 chr9: 126,375,297-126,622,635	LMX1B, LMX1B-DT, 3 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
nsv4384085	copy number variation	1	nstd173	human		GRCh37 chr9: 128,623,691-129,527,711 , GRCh38.p12 chr9: 125,861,412-126,765,432	NRON, MVB12B, 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
nsv3924370	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225	MVB12B, MIR4672, 97 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
nsv3921944	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 126,081,595-127,781,685 , NCBI36 chr9: 127,883,695-129,583,785 , GRCh37 chr9: 128,843,874-130,543,964	LOC101929116, LRSAM1, 30 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

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Number of Variants: 20

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