dbVar for Gene (Select 353091) - 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
nsv5102359	mobile element insertion	1	nstd203	human		GRCh38 chr6: 149,915,078-149,915,101 , GRCh37.p13 chr6: 150,236,214-150,236,237	RAET1E-AS1, RAET1G
nsv4675234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929	RNU7-3P, HSPD1P16, 86 more genes
nsv4456488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222	PDCL3P5, SYTL3, 176 more genes
nsv4436722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,690,764-150,494,873 , GRCh38.p12 chr6: 148,369,628-150,173,737	PCMT1, ULBP3, 42 more genes
nsv4330897	inversion	1	nstd166	human		GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351	, ACAT2, 894 more genes
nsv4146169	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 150,243,347-150,243,437 , GRCh38.p12 chr6: 149,922,211-149,922,301	RAET1G
nsv4144398	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 150,230,529-150,278,806 , GRCh38.p12 chr6: 149,909,393-149,957,670	RAET1E-AS1, RAET1G, 3 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	UST-AS2, LOC729681, 394 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	PPP1R14C, RAET1K, 107 more genes
nsv3919153	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 147,943,180-150,590,792 , GRCh37 chr6: 147,901,487-150,549,099 , GRCh38 chr6: 147,580,351-150,227,963	PHB1P1, RAET1M, 45 more genes
nsv3918368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,126,255-151,214,851 , GRCh38 chr6: 147,805,119-150,893,715 , NCBI36 chr6: 148,167,948-151,256,544	CYP51A1P3, SNRPEP6, 52 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	KATNA1, RNF217-AS1, 422 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	LOC105369171, SHPRH, 418 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	HYMAI, SMIM28, 263 more genes
nsv3910985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 146,843,948-151,790,457 , GRCh37 chr6: 146,802,255-151,748,764 , GRCh38 chr6: 146,481,119-151,427,629	RMND1, LOC645967, 77 more genes
nsv3904637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,947,731-150,266,155 , GRCh38.p12 chr6: 144,626,595-149,945,019	LOC107986660, CCT7P1, 59 more genes
nsv3891146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095	UST, RAET1K, 131 more genes
nsv3890752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870	LOC105378052, RNU6-302P, 109 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ITPR3, HSD17B8, 2905 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SOD1P1, HLA-DPB1, 2905 more genes

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Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 107

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Number of Variants: 20

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