dbVar for Gene (Select 100616119) - 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
nsv4729098	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 130,128,323-134,938,470 , GRCh38.p12 chr11: 130,258,428-135,068,576	BAK1P2, OPCML, 56 more genes
nsv4729012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576	LINC02706, APLP2, 92 more genes
nsv4728891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576	ARHGAP32, NAP1L1P1, 125 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
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
nsv4675571	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 131,327,161-134,938,470 , GRCh38.p12 chr11: 131,457,267-135,068,576	SNORD153, LOC105369587, 33 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
nsv4455332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 130,969,272-134,938,470 , GRCh38.p12 chr11: 131,099,377-135,068,576	LOC107984412, LINC02743, 36 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
nsv4350042	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 125,446,101-134,904,063 , GRCh38.p12 chr11: 125,576,205-135,034,169	SNX19, TP53AIP1, 138 more genes
nsv4349788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 133,325,079-134,157,243 , GRCh38.p12 chr11: 133,455,184-134,287,349	LINC02743, IGSF9B, 15 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
nsv3924653	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 126,979,765-134,373,558 , GRCh38 chr11: 127,604,660-134,998,454 , GRCh37 chr11: 127,474,555-134,868,348	ZNF123P, ST14, 91 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
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
nsv3923345	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 127,564,482-135,075,271 , GRCh37 chr11: 127,434,377-134,945,165 , NCBI36 chr11: 126,939,587-134,450,377	LINC01395, LOC100507548, 93 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

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Has Clinical Interpretation

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Items: 1 to 20 of 196

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Number of Variants: 20

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