plaat3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 10

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	PLAAT3, FAUP4, 2031 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	PLAAT3, 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	PLAAT3, 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	PLAAT3, 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	PLAAT3, PYGM, 2125 more genes
nsv3924003	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 62,417,274-63,859,091 , GRCh37 chr11: 62,660,698-64,102,515 , GRCh38 chr11: 62,893,226-64,335,043	PLAAT3, BAD, 58 more genes
nsv3895156	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 63,064,163-63,343,322 , GRCh38.p12 chr11: 63,296,691-63,575,850	PLAAT3, PLAAT2, 8 more genes
nsv3901321	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 63,230,830-63,342,467 , GRCh38.p12 chr11: 63,463,358-63,574,995	PLAAT3, LGALS12, 6 more genes
nsv7093694	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878	PLAAT3, VPS37C, 298 more genes
nsv4729316	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 62,714,816-63,383,226 , GRCh38.p12 chr11: 62,947,344-63,615,754	PLAAT3, LOC105369334, 18 more genes

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