dbVar for Gene (Select 653483) - 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
nsv7148156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878	LOC105378126, LOC107986550, 149 more genes
nsv7137133	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590	LOC101929460, GPR31, 199 more genes
nsv7052981	inversion	1	nstd229	human		GRCh38 chr6: 167,557,448-168,005,975 , GRCh37.p13 chr6: 168,042,074-168,406,655	LINC01558, LOC105378130, 12 more genes
nsv7051730	inversion	1	nstd229	human		GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278	WDR27, KIF25, 49 more genes
nsv7040499	inversion	1	nstd229	human		GRCh38 chr6: 167,795,352-167,865,259 , GRCh37.p13 chr6: 168,196,032-168,265,939	AFDN-DT, AFDN, 2 more genes
nsv7038888	inversion	1	nstd229	human		GRCh38 chr6: 167,222,887-168,363,767 , GRCh37.p13 chr6: 167,636,375-168,764,447	LOC101929420, LOC102724220, 32 more genes
nsv6817934	copy number variation	1	nstd229	human		GRCh38 chr6: 167,045,707-167,831,746 , GRCh37.p13 chr6: 167,459,195-168,232,426	LOC105378123, LOC105378126, 28 more genes
nsv6636689	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394	GNG5P1, LINC01558, 144 more genes
nsv6634373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581	LOC107986547, LOC107986550, 132 more genes
nsv6315428	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394	TBP, LOC105378130, 200 more genes
nsv6315394	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 167,770,398-170,919,482 , GRCh38.p12 chr6: 167,356,910-170,610,394	LINC02544, LOC107986676, 72 more genes
nsv6313815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 167,317,903-170,919,482 , GRCh38.p12 chr6: 166,904,415-170,610,394	LOC285804, LOC105378149, 91 more genes
nsv6313793	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,212,864-170,919,482 , GRCh38.p12 chr6: 161,791,832-170,610,394	LOC645468, GPR31, 148 more genes
nsv6313745	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,290,087-170,919,482 , GRCh38.p12 chr6: 162,869,055-170,610,394	HGC6.3, LOC112267970, 143 more genes
nsv6313560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394	LOC105378142, LOC100289495, 159 more genes
nsv6291387	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,051,206-170,919,482 , GRCh38.p12 chr6: 167,650,526-170,610,394	LINC02544, LINC02487, 64 more genes
nsv6136487	copy number variation	1	nstd213	human		GRCh37 chr6: 168,050,000-168,840,001 , GRCh38.p12 chr6: 167,649,320-168,439,321	FRMD1, LINC02487, 22 more genes
nsv5543028	insertion	1	nstd206	human		GRCh38 chr6: 167,826,835-167,826,858 , GRCh37.p13 chr6: 168,227,515-168,227,538	AFDN, AFDN-DT
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

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Has Clinical Interpretation

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Items: 1 to 20 of 209

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Number of Variants: 20

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