dbVar for Gene (Select 401288) - 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
nsv5168100	mobile element insertion	1	nstd203	human		GRCh38 chr6: 169,790,915-169,790,926 , GRCh37.p13 chr6: 170,191,011-170,191,022	LINC00574, LINC00242
nsv4966055	copy number variation	1	nstd200	human		GRCh38 chr6: 169,795,377-169,799,438 , GRCh37.p13 chr6: 170,195,473-170,199,534	LINC00574, LINC00242
nsv4966027	copy number variation	1	nstd200	human		GRCh38 chr6: 169,180,752-170,050,020 , GRCh37.p13 chr6: 169,580,847-170,365,244	, LOC100131532, 17 more genes
nsv4729645	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394	CCR6, GNG5P1, 118 more genes
nsv4729261	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394	LOC107986549, AFDN, 81 more genes
nsv4675958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 167,440,417-170,919,482 , GRCh38.p12 chr6: 167,026,929-170,610,394	CCR6, HGC6.3, 86 more genes
nsv4675923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394	TRE-TTC15-1, LOC105378137, 148 more genes
nsv4675577	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 170,136,337-170,919,482 , GRCh38.p12 chr6: 169,736,241-170,610,394	LOC107986676, LOC105378149, 22 more genes
nsv4675281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394	LOC105378127, LOC105378130, 148 more genes
nsv4455397	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394	TBP, LOC112267970, 108 more genes
nsv4436131	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067	ACAT2, CCR6, 303 more genes
nsv4376081	copy number variation	1	nstd173	human		GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394	, LOC107986550, 151 more genes
nsv4350147	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,311,806-170,881,789 , GRCh38.p12 chr6: 167,911,126-170,572,701	LINC00574, LOC107986674, 56 more genes
nsv4349604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 166,517,762-170,919,470 , GRCh38.p12 chr6: 166,104,274-170,610,382	LOC105378145, FRMD1, 109 more genes
nsv4347933	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 162,966,301-170,914,973 , GRCh38.p12 chr6: 162,545,269-170,605,885	CCR6, GNG5P1, 146 more genes
nsv4136193	copy number variation	1	nstd166	human		GRCh37.p13 chr6: 170,179,000-170,240,000 , GRCh38.p12 chr6\|NT_187552.1: 54,106-115,106 , GRCh38.p12 chr6: 169,778,904-169,839,904	ERMARD, LINC00574, 1 more genes
nsv3923088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,246,945-170,921,089 , NCBI36 chr6: 160,166,935-170,763,014 , GRCh38 chr6: 159,825,913-170,612,001	DKFZp451B082, LOC107986548, 169 more genes
nsv3923019	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,924,849-170,921,089 , NCBI36 chr6: 168,667,698-170,763,014 , GRCh38 chr6: 168,524,169-170,612,001	LOC107986674, LINC02519, 41 more genes
nsv3922967	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 169,023,487-170,753,165 , GRCh38 chr6: 168,881,467-170,602,152 , GRCh37 chr6: 169,281,562-170,911,240	LOC105378153, LOC105378150, 36 more genes
nsv3922779	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 169,700,088-169,985,938 , GRCh37.p13 chr6: 169,958,163-170,244,013 , GRCh38.p12 chr6: 169,558,067-169,843,917	LINC00574, LINC00242, 5 more genes

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Items: 1 to 20 of 197

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Number of Variants: 20

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