dbVar for Gene (Select 245806) - 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
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
nsv4948368	copy number variation	1	nstd200	human		GRCh38 chr6: 117,266,325-117,267,299 , GRCh37.p13 chr6: 117,587,488-117,588,462	VGLL2
nsv4768325	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959	GJA1, RNU4-76P, 80 more genes
nsv4729273	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 117,190,128-117,881,578 , GRCh38.p12 chr6: 116,868,965-117,560,415	LOC105377964, RN7SKP18, 10 more genes
nsv4457007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231	HDAC2-AS2, NIP7P3, 134 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
nsv4143251	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 117,587,488-117,588,462 , GRCh38.p12 chr6: 117,266,325-117,267,299	VGLL2
nsv4136962	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 117,272,241-117,681,595 , GRCh38.p12 chr6: 116,951,078-117,360,432	ROS1, VGLL2, 5 more genes
nsv3942261	insertion	1	nstd167	human		GRCh37 chr6: 117,594,846-117,594,846 , GRCh38.p12 chr6: 117,273,683-117,273,683	VGLL2
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
nsv3924661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162	MCM9, YWHAZP4, 146 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
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
nsv3919913	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 117,634,847-118,309,698 , GRCh37 chr6: 117,528,154-118,203,005 , GRCh38 chr6: 117,206,991-117,881,842	RAP1BP3, DCBLD1, 10 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
nsv3919038	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 117,243,055-120,081,740 , GRCh37 chr6: 117,136,362-120,040,041 , GRCh38 chr6: 116,815,199-119,718,887	MAN1A1, PLN, 37 more genes
nsv3918326	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 116,145,074-123,993,898 , GRCh37.p13 chr6: 116,038,381-123,952,199 , GRCh38.p12 chr6: 115,717,217-123,631,054	MCM9, FRK, 93 more genes
nsv3911999	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 115,754,819-118,363,096 , GRCh37 chr6: 115,648,126-118,256,403 , GRCh38 chr6: 115,326,962-117,935,240	COL10A1, FRK, 40 more genes
nsv3910417	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300	LINC02518, LOC105377937, 266 more genes
nsv3906984	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 112,069,445-120,994,664 , GRCh38.p12 chr6: 111,748,242-120,673,518	COL10A1, FRK, 115 more genes

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Has Clinical Interpretation

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Number of Variants: 20

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