dbVar for Gene (Select 283159) - 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
nsv4981116	copy number variation	1	nstd200	human		GRCh38 chr11: 124,309,404-124,312,953 , GRCh37.p13 chr11: 124,179,300-124,182,849	OR8D1
nsv4981114	copy number variation	1	nstd200	human		GRCh38 chr11: 124,263,058-124,406,681 , GRCh37.p13 chr11: 124,132,954-124,276,577	SLC5A4P1, OR8C1P, 12 more genes
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
nsv4201747	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 124,173,680-124,180,770 , GRCh38.p12 chr11: 124,303,784-124,310,874	OR8D1
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
nsv3922662	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 123,670,646-134,868,420 , GRCh38 chr11: 123,799,938-134,998,526 , NCBI36 chr11: 123,175,856-134,373,630	SNORD153, PATE3, 219 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
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
nsv3918536	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 123,581,142-134,373,630 , GRCh38 chr11: 124,205,225-134,998,526 , GRCh37 chr11: 124,075,932-134,868,420	LOC100533644, NFRKB, 197 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

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Number of Variants: 20

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