dbVar for Gene (Select 101929227) - 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
nsv5663611	insertion	1	nstd207	human		GRCh38 chr11: 120,876,376-120,876,376 , GRCh37.p13 chr11: 120,747,085-120,747,085	LOC101929227, GRIK4
nsv5653588	insertion	1	nstd207	human		GRCh38 chr11: 120,876,107-120,876,107 , GRCh37.p13 chr11: 120,746,816-120,746,816	LOC101929227, GRIK4
nsv5511387	copy number variation	1	nstd206	human		GRCh38 chr11: 120,884,557-120,884,634 , GRCh37.p13 chr11: 120,755,266-120,755,343	LOC101929227, GRIK4
nsv4766716	insertion	1	nstd199	human		GRCh37 chr11: 120,747,086-120,747,086 , GRCh38.p12 chr11: 120,876,377-120,876,377	GRIK4, LOC101929227
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
nsv4448108	insertion	1	nstd175	human		GRCh37 chr11: 120,746,822-120,746,822 , GRCh38.p12 chr11: 120,876,113-120,876,113	GRIK4, LOC101929227
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
nsv3970204	insertion	1	nstd168	human		GRCh38 chr11: 120,854,004-120,892,231 , GRCh37.p13 chr11: 120,724,713-120,762,940	GRIK4, LOC101929227
nsv3936575	insertion	1	nstd167	human		GRCh37 chr11: 120,747,085-120,747,085 , GRCh38.p12 chr11: 120,876,376-120,876,376	GRIK4, LOC101929227
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
nsv3922395	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 120,453,168-121,182,251 , NCBI36 chr11: 119,829,087-120,558,170 , GRCh37 chr11: 120,323,877-121,052,960	HMGB1P42, GRIK4, 8 more genes

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Number of Variants: 20

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