dbVar for Gene (Select 100874281) - 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
nsv5972430	insertion	1	nstd209	human		GRCh38 chr11: 132,282,976-132,282,976 , GRCh37.p13 chr11: 132,152,870-132,152,870	NTM, NTM-IT
nsv5504638	copy number variation	1	nstd206	human		GRCh38 chr11: 132,280,795-132,294,755 , GRCh37.p13 chr11: 132,150,689-132,164,649	NTM, NTM-IT
nsv4987749	copy number variation	1	nstd200	human		GRCh38 chr11: 132,280,689-132,288,810 , GRCh37.p13 chr11: 132,150,583-132,158,704	NTM, NTM-IT
nsv4987748	copy number variation	1	nstd200	human		GRCh38 chr11: 132,270,954-132,286,699 , GRCh37.p13 chr11: 132,140,848-132,156,593	NTM-IT, NTM
nsv4729658	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 131,535,422-133,318,785 , GRCh38.p12 chr11: 131,665,528-133,448,890	LOC100419058, NTM-IT, 4 more genes
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
nsv4675420	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 131,970,312-132,216,061 , GRCh38.p12 chr11: 132,100,418-132,346,167	NTM, NTM-IT
nsv4675223	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 131,855,168-133,236,931 , GRCh38.p12 chr11: 131,985,274-133,367,036	NTM, OPCML, 2 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
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

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Organism

Variant Type

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 203

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Number of Variants: 20

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