dbVar for Gene (Select 80007) - 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
nsv6112765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815	STK32C, LOC105378542, 266 more genes
nsv5980446	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718	LINC02641, CFAP46, 194 more genes
nsv5721620	mobile element insertion	1	nstd211	human		GRCh38 chr10: 122,944,869-122,944,869 , GRCh37.p13 chr10: 124,704,385-124,704,385	C10orf88
nsv5672603	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789	ACADSB, DMBT1, 84 more genes
nsv5498833	copy number variation	1	nstd206	human		GRCh38 chr10: 122,931,909-122,931,985 , GRCh37.p13 chr10: 124,691,425-124,691,501	C10orf88
nsv5493998	copy number variation	1	nstd206	human		GRCh38 chr10: 122,950,755-122,951,352 , GRCh37.p13 chr10: 124,710,271-124,710,868	C10orf88
nsv5373311	translocation	1	nstd200	human		GRCh38 chr10: 122,951,352-122,951,352 , GRCh38 chr10: 122,950,755-122,950,755 , GRCh37.p13 chr10: 124,710,271-124,710,271 , GRCh37.p13 chr10: 124,710,868-124,710,868	C10orf88
nsv5354536	translocation	1	nstd200	human		GRCh38 chr10: 122,946,043-122,946,043 , GRCh38 chr10: 122,945,985-122,945,985 , GRCh37.p13 chr10: 124,705,559-124,705,559 , GRCh37.p13 chr10: 124,705,501-124,705,501	C10orf88
nsv5335636	translocation	1	nstd200	human		GRCh37 chr10: 124,705,559-124,705,559 , GRCh37 chr10: 124,705,501-124,705,501 , GRCh38.p12 chr10: 122,946,043-122,946,043 , GRCh38.p12 chr10: 122,945,985-122,945,985	C10orf88
nsv4679699	copy number variation	1	nstd189	human		GRCh37.p13 chr10: 124,478,359-125,318,025 , GRCh38.p12 chr10: 122,718,843-123,558,509	ACADSB, HMX2, 15 more genes
nsv4675991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639	STK32C, LOC105378542, 237 more genes
nsv4481739	mobile element insertion	1	nstd166	human		GRCh37.p13 chr10: 124,691,011-124,691,011 , GRCh38.p12 chr10: 122,931,495-122,931,495	C10orf88
nsv4456626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639	LOC105378521, ZRANB1, 317 more genes
nsv4349508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290	PRLHR, LOC105378513, 121 more genes
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	LOC105378492, VENTX, 373 more genes
nsv4210639	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 124,710,271-124,710,868 , GRCh38.p12 chr10: 122,950,755-122,951,352	C10orf88
nsv4208989	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 123,721,898-126,209,916 , GRCh38.p12 chr10: 121,962,383-124,521,347	, CHST15, 44 more genes
nsv4203134	copy number variation	1	nstd166	human		GRCh37.p13 chr10: 124,689,198-124,689,771 , GRCh38.p12 chr10: 122,929,682-122,930,255	C10orf88
nsv3924720	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133	OR6L2P, RPL19P16, 208 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	AS-PTPRE, SFXN4, 330 more genes

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Items: 1 to 20 of 131

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Number of Variants: 20

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