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

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3893064	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 59,383,325-59,383,735 , GRCh38.p12 chr11: 59,615,852-59,616,262	OSBP, LOC101927226
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	OSBP, 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	OSBP, 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	OSBP, 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	OSBP, 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	OSBP, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	OSBP, TRR-TCT3-2, 494 more genes
nsv3890886	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184	OSBP, MYRF, 137 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	OSBP, VPS37C, 298 more genes

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osbp[All Fields] AND 1[has_clinical] (10)
dbVar
Homo sapiens G protein-coupled receptor 68, mRNA (cDNA clone IMAGE:6971809), par...
Homo sapiens G protein-coupled receptor 68, mRNA (cDNA clone IMAGE:6971809), partial cds
gi|45768629|gb|BC067472.1|

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