aldh3b2[All Fields] AND 1[has_clinical] - 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
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	ALDH3B2, FAUP4, 2031 more genes
nsv3921639	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669	ALDH3B2, MIR6860, 106 more genes
nsv3915534	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 66,970,200-68,203,117 , GRCh38 chr11: 67,446,153-68,679,073 , GRCh37 chr11: 67,213,624-68,446,541	ALDH3B2, LOC107984343, 46 more genes
nsv3917536	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 66,409,957-67,222,297 , GRCh38 chr11: 66,885,910-67,698,250 , GRCh37 chr11: 66,653,381-67,465,721	ALDH3B2, PPP1CA, 39 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	ALDH3B2, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	ALDH3B2, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	ALDH3B2, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	ALDH3B2, PYGM, 2125 more genes
nsv4349000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931	ALDH3B2, SNORD13F, 141 more genes
nsv3911732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 66,193,502-67,890,770 , GRCh37 chr11: 65,960,973-67,658,241 , NCBI36 chr11: 65,717,549-67,414,817	ALDH3B2, B4GAT1, 90 more genes
nsv3920906	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598	ALDH3B2, GRK2, 82 more genes
nsv3907435	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 67,349,872-67,715,028 , GRCh38.p12 chr11: 67,582,401-67,947,557	ALDH3B2, LOC105369359, 21 more genes
nsv3896688	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 67,331,526-67,693,404 , GRCh38.p12 chr11: 67,564,055-67,925,933	ALDH3B2, GSTP1, 20 more genes
nsv3918462	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 67,114,780-67,222,297 , GRCh38 chr11: 67,590,733-67,698,250 , GRCh37 chr11: 67,358,204-67,465,721	ALDH3B2, DOC2GP, 6 more genes
nsv7094093	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473	ALDH3B2, B4GAT1, 208 more genes
nsv3904873	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 66,024,774-67,430,781 , GRCh38.p12 chr11: 66,257,303-67,663,310	ALDH3B2, B4GAT1-DT, 79 more genes
nsv4675137	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043	ALDH3B2, PPP1CA, 58 more genes
nsv4455772	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 67,081,259-67,471,729 , GRCh38.p12 chr11: 67,313,788-67,704,258	ALDH3B2, LOC100130987, 27 more genes
nsv3922289	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 67,590,733-67,806,931 , NCBI36 chr11: 67,114,780-67,330,978 , GRCh37 chr11: 67,358,204-67,574,402	ALDH3B2, NDUFV1-DT, 13 more genes
nsv3888150	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 67,373,669-67,588,012 , GRCh38 chr11: 67,606,198-67,820,541	ALDH3B2, OR7E145P, 14 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 21

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Number of Variants: 20

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Search details

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