dbVar for Gene (Select 2830) - 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
nsv5564516	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235	RN7SL617P, METTL24, 67 more genes
nsv5038830	inversion	1	nstd200	human		GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814	, LOC105377981, 623 more genes
nsv4945539	copy number variation	1	nstd200	human		GRCh38 chr6: 109,978,313-109,978,770 , GRCh37.p13 chr6: 110,299,516-110,299,973	GPR6
nsv4768376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741	LOC101927405, GPR6, 211 more genes
nsv4728858	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,288,308-110,768,384 , GRCh38.p12 chr6: 109,967,105-110,447,181	METTL24, LOC105377936, 9 more genes
nsv4685989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082	RPL23AP50, RNU6-960P, 216 more genes
nsv4674911	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 109,564,694-112,232,351 , GRCh38.p12 chr6: 109,243,491-111,911,148	LOC105377939, LOC105377945, 57 more genes
nsv4611628	copy number variation	1	nstd183	human		GRCh37 chr6: 110,102,601-110,360,790 , GRCh38.p12 chr6: 109,781,398-110,039,587	, GPR6, 2 more genes
nsv4387301	copy number variation	1	nstd173	human		GRCh37 chr6: 110,028,988-110,370,868 , GRCh38.p12 chr6: 109,707,785-110,049,665	, LOC107986631, 2 more genes
nsv4386846	copy number variation	2	nstd173	human		GRCh37 chr6: 110,098,753-110,370,641 , GRCh38.p12 chr6: 109,777,550-110,049,438	, FIG4, 2 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
nsv4312499	inversion	1	nstd166	human		GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456	, CRYBG1, 284 more genes
nsv3924741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058	LOC105377979, LOC105377936, 266 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	TUBE1, PLN, 318 more genes
nsv3922965	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 109,695,677-110,409,939 , GRCh37.p13 chr6: 109,588,984-110,303,246 , GRCh38.p12 chr6: 109,267,781-109,982,043	AK9, PPIL6, 11 more genes
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	SSXP10, TRE-CTC1-7, 298 more genes
nsv3919897	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239	HACE1, RNU6-1144P, 174 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	RNU6-770P, MAP3K5-AS2, 810 more genes
nsv3917185	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 107,873,178-110,975,803 , GRCh38 chr6: 107,445,281-110,547,907 , GRCh37 chr6: 107,766,485-110,869,110	SMPD2, RPS12P13, 56 more genes
nsv3914025	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 107,798,038-116,255,339 , GRCh38 chr6: 107,370,141-115,827,482 , GRCh37 chr6: 107,691,345-116,148,646	TRAF3IP2-AS1, RPS12P13, 139 more genes

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 114

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Number of Variants: 20

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