dbVar for Gene (Select 9324) - 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
nsv5845455	copy number variation	1	nstd209	human		GRCh38 chr6: 79,217,039-79,219,138 , GRCh37.p13 chr6: 79,926,756-79,928,855	HMGN3
nsv5683290	mobile element insertion	1	nstd211	human		GRCh38 chr6: 79,201,131-79,201,131 , GRCh37.p13 chr6: 79,910,848-79,910,848	HMGN3
nsv5468446	copy number variation	1	nstd206	human		GRCh38 chr6: 79,085,471-79,214,395 , GRCh37.p13 chr6: 79,795,188-79,924,112	HMGN3
nsv5396453	mobile element insertion	1	nstd206	human		GRCh38 chr6: 79,201,131-79,201,182 , GRCh37.p13 chr6: 79,910,848-79,910,899	HMGN3
nsv5369334	translocation	1	nstd200	human		GRCh38 chr6: 79,213,798-79,213,798 , GRCh38 chr6: 79,213,238-79,213,238 , GRCh37.p13 chr6: 79,922,955-79,922,955 , GRCh37.p13 chr6: 79,923,515-79,923,515	HMGN3
nsv4941718	copy number variation	1	nstd200	human		GRCh38 chr6: 79,216,580-79,225,666 , GRCh37.p13 chr6: 79,926,297-79,935,383	HMGN3
nsv4729340	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320	LOC107986613, LOC101928516, 58 more genes
nsv4456122	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,216,253-82,753,743 , GRCh38.p12 chr6: 77,506,536-82,044,026	LOC105377869, AK4P5, 38 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	HLA-DPB2, CIMIP3, 1001 more genes
nsv4143220	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 79,922,955-79,923,515 , GRCh38.p12 chr6: 79,213,238-79,213,798	HMGN3
nsv4139917	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 79,909,011-79,909,316 , GRCh38.p12 chr6: 79,199,294-79,199,599	HMGN3
nsv4137808	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 79,926,297-79,935,383 , GRCh38.p12 chr6: 79,216,580-79,225,666	HMGN3
nsv3924632	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 78,661,176-80,245,532 , NCBI36 chr6: 79,427,612-81,011,968 , GRCh37 chr6: 79,370,893-80,955,249	LOC107986613, LCA5, 23 more genes
nsv3924180	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510	LOC105377875, KCNQ5-IT1, 188 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	SPACA1, TAF13P1, 187 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
nsv3911622	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 79,678,455-84,862,865 , GRCh37.p13 chr6: 79,621,736-84,806,146 , GRCh38.p12 chr6: 78,912,019-84,096,427	BCKDHB, DBIP1, 55 more genes
nsv3911072	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 78,459,366-80,488,945 , GRCh37.p13 chr6: 78,402,647-80,432,226 , GRCh38.p12 chr6: 77,692,930-79,722,509	LOC100418713, LOC107986613, 16 more genes
nsv3889959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055	MRAP2, LCA5, 125 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

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Items: 1 to 20 of 151

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Number of Variants: 20

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