dbVar for Gene (Select 54538) - 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
nsv5261402	copy number variation	1	nstd204	human		GRCh38.p13 chr11: 124,884,264-124,885,563 , GRCh37.p13 chr11: 124,754,160-124,755,459	ROBO4
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
nsv4718353	mobile element insertion	1	nstd186	human		GRCh37 chr11: 124,751,627-124,751,627 , GRCh38.p12 chr11: 124,881,731-124,881,731	ROBO4, ROBO3
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
nsv4675674	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576	FAM118B, PUS3, 184 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
nsv4673961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583	OR8A2P, LOC101929473, 186 more genes
nsv4616806	copy number variation	1	nstd183	human		GRCh37 chr11: 124,700,218-124,829,319 , GRCh38.p12 chr11: 124,830,322-124,959,423	ROBO4, ROBO3, 6 more genes
nsv4606555	copy number variation	1	nstd183	human		GRCh37 chr11: 124,692,835-125,311,674 , GRCh38.p12 chr11: 124,822,939-125,441,778	HEPN1, TMEM218, 14 more genes
nsv4508618	mobile element insertion	1	nstd166	human		GRCh37.p13 chr11: 124,751,627-124,751,627 , GRCh38.p12 chr11: 124,881,731-124,881,731	ROBO3, ROBO4
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
nsv3968664	insertion	1	nstd168	human		GRCh38 chr11: 124,882,223-124,894,111 , GRCh37.p13 chr11: 124,752,119-124,764,007	ROBO4, LOC107984406
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
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

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Has Clinical Interpretation

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Items: 1 to 20 of 175

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Number of Variants: 20

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