dbVar for Gene (Select 390260) - 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
nsv4732750	copy number variation	1	nstd199	human		GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572	, LINC02702, 392 more genes
nsv4675832	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576	MIR8052, BLID, 275 more genes
nsv4674572	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571	ACRV1, APLP2, 382 more genes
nsv4455281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576	NTM-AS1, LOC403312, 369 more genes
nsv4436748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169	LINC02098, LOC105369587, 276 more genes
nsv4349506	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591	LOC107984407, DCPS, 394 more genes
nsv4349045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169	MPZL3, ADAMTS8, 393 more genes
nsv3924566	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160	CCDC15-DT, LOC105369544, 271 more genes
nsv3923916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,296,802-124,641,109 , NCBI36 chr11: 119,802,012-124,146,319 , GRCh38 chr11: 120,426,093-124,771,213	OR8B2, OR8G5, 120 more genes
nsv3923375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526	VPS26B, LOC105369531, 390 more genes
nsv3923251	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165	KIRREL3-AS3, OR8B4, 279 more genes
nsv3922773	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617	ETS1-AS1, SLC37A2, 301 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	RPS27P19, UBASH3B, 655 more genes
nsv3921036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 123,058,272-123,670,848 , GRCh38 chr11: 123,187,564-123,800,140 , NCBI36 chr11: 122,563,482-123,176,058	SCN3B, SF3A3P2, 12 more genes
nsv3919969	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 121,780,459-135,075,271 , GRCh37 chr11: 121,651,167-134,945,165 , NCBI36 chr11: 121,156,377-134,450,377	STT3A-AS1, RNU6-876P, 262 more genes
nsv3918400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,482,185-134,938,470 , GRCh38 chr11: 121,611,476-135,068,576 , NCBI36 chr11: 120,987,395-134,443,680	RN7SL167P, LOC107984409, 262 more genes
nsv3917453	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 120,236,432-135,040,246 , NCBI36 chr11: 119,612,351-134,415,350 , GRCh37 chr11: 120,107,141-134,910,140	LOC105369577, MIR100, 283 more genes
nsv3916857	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513	RPUSD4, ELOCP22, 390 more genes
nsv3916826	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 118,559,939-134,452,384 , GRCh37.p13 chr11: 119,054,729-134,946,516 , GRCh38.p12 chr11: 119,184,020-135,076,622	NECTIN1-DT, TP53AIP1, 317 more genes
nsv3915852	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 122,919,567-124,177,307 , GRCh37 chr11: 123,414,357-124,672,097 , GRCh38 chr11: 123,543,649-124,802,201	OR10G8, OR8Q1P, 69 more genes

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Items: 1 to 20 of 121

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Number of Variants: 20

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