dbVar for Gene (Select 3298) - 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
nsv5906366	copy number variation	1	nstd209	human		GRCh38 chr6: 122,228,486-122,547,637 , GRCh37.p13 chr6: 122,549,632-122,868,782	HSF2, PKIB, 1 more genes
nsv5112478	mobile element insertion	1	nstd203	human		GRCh38 chr6: 122,420,700-122,420,729 , GRCh37.p13 chr6: 122,741,845-122,741,874	HSF2
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
nsv4933839	copy number variation	1	nstd200	human		GRCh38 chr6: 122,432,740-122,451,069 , GRCh37.p13 chr6: 122,753,885-122,772,214	HSF2, SERINC1
nsv4933838	copy number variation	1	nstd200	human		GRCh38 chr6: 122,413,863-122,415,118 , GRCh37.p13 chr6: 122,735,008-122,736,263	HSF2
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
nsv4524266	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 122,019,997-123,515,000 , GRCh38.p12 chr6: 121,698,851-123,193,855	, LOC105377979, 11 more genes
nsv4489407	mobile element insertion	1	nstd166	human		GRCh37.p13 chr6: 122,739,430-122,739,430 , GRCh38.p12 chr6: 122,418,285-122,418,285	HSF2
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
nsv4144765	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 122,678,574-122,743,113 , GRCh38.p12 chr6: 122,357,429-122,421,968	HSF2
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
nsv3924512	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 118,035,003-127,062,818 , GRCh37 chr6: 117,928,310-127,021,125 , GRCh38 chr6: 117,607,147-126,699,980	HSF2, LOC285762, 85 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
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
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
nsv3914300	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 119,337,879-126,076,146 , GRCh38 chr6: 118,975,015-125,713,307 , GRCh37 chr6: 119,296,180-126,034,453	RNF217-AS1, NKAIN2, 50 more genes
nsv3913689	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272	TPD52L1, MESTP1, 316 more genes
nsv3910532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 122,150,762-126,475,618 , GRCh38 chr6: 121,829,616-126,154,472 , NCBI36 chr6: 122,192,461-126,517,311	LOC105377982, NCOA7, 32 more genes
nsv3893140	copy number variation	1	nstd102	human	drug response	GRCh37 chr6: 112,939,290-132,327,952 , GRCh38.p12 chr6: 112,618,088-132,006,812	LOC105377998, TBC1D32, 220 more genes

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Number of Variants: 20

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Items: 1 to 20 of 154

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Number of Variants: 20

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