dbVar for Gene (Select 338470) - 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
nsv5968494	inversion	1	nstd209	human		GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043	, ARG1, 137 more genes
nsv5906945	copy number variation	1	nstd209	human		GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534	, LOC105377999, 105 more genes
nsv5673525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 129,204,381-129,837,502 , GRCh38.p12 chr6: 128,883,236-129,516,357	MESTP1, LOC102723409, 3 more genes
nsv5464607	copy number variation	1	nstd206	human		GRCh38 chr6: 128,624,100-129,882,235 , GRCh37.p13 chr6: 128,945,245-130,203,380	LAMA2, LOC102723409, 10 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
nsv4676074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 128,808,063-129,473,811 , GRCh38.p12 chr6: 128,486,918-129,152,666	PTPRK, MESTP1, 4 more genes
nsv4455533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 129,236,792-129,488,075 , GRCh38.p12 chr6: 128,915,647-129,166,930	BMPR1AP1, MESTP1, 1 more genes
nsv4453203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 129,204,381-129,419,570 , GRCh38 chr6: 128,883,236-129,098,425	LAMA2, MESTP1
nsv4378998	copy number variation	1	nstd173	human		GRCh37 chr6: 128,889,640-129,953,317 , GRCh38.p12 chr6: 128,568,495-129,632,172	MESTP1, EEF1DP5, 7 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
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
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
nsv3914024	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 126,857,372-132,860,687 , GRCh37 chr6: 126,815,679-132,818,994 , GRCh38 chr6: 126,494,533-132,497,855	ARG1, CCN2, 74 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
nsv3911415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 126,576,700-129,752,871 , GRCh38 chr6: 126,255,554-129,431,726 , NCBI36 chr6: 126,618,393-129,794,564	LOC100420743, RNA5SP217, 38 more genes
nsv3911176	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 127,884,866-129,373,079 , GRCh37.p13 chr6: 127,843,173-129,331,386 , GRCh38.p12 chr6: 127,522,028-129,010,241 , GRCh38.p12 chr6\|NT_187556.1: 1-870,480	PTPRK, LAMA2, 13 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
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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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 101

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Number of Variants: 20

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