OSC8170 AND nstd224 - 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
nsv6630203	copy number variation	32	nstd224	human		GRCh37 chr5: 104,432,296-104,494,569 , GRCh38.p12 chr5: 105,096,595-105,158,868	RAB9BP1
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6627632	copy number variation	2	nstd224	human		GRCh37 chr2: 228,243,028-228,258,199 , GRCh38.p12 chr2: 227,378,312-227,393,483	TM4SF20
nsv6633836	copy number variation	4	nstd224	human		GRCh37 chrX: 140,697,115-140,779,598 , GRCh38.p12 chrX: 141,608,987-141,691,441	SPANXA2-OT1, LOC645188
nsv6624676	copy number variation	1	nstd224	human		GRCh37 chr19: 14,139,004-14,154,122 , GRCh38.p12 chr19: 14,028,192-14,043,310	IL27RA, RLN3
nsv6620263	copy number variation	26	nstd224	human		GRCh37 chr10: 135,252,932-135,376,669 , GRCh38.p12 chr10: 133,439,428-133,563,165	CYP2E1, SYCE1, 3 more genes
nsv6627000	copy number variation	1	nstd224	human		GRCh37 chr21: 31,176,283-31,687,009 , GRCh38.p12 chr21: 29,803,966-30,314,691	GRIK1, CLDN8, 5 more genes
nsv6625838	copy number variation	91	nstd224	human		GRCh37 chr1: 149,036,931-149,332,177 , GRCh38.p12 chr1: 143,542,264-143,837,623	LINC02591, NBPF17P, 19 more genes
nsv6623606	copy number variation	28	nstd224	human		GRCh37 chr16: 32,509,483-33,615,125 , GRCh38.p12 chr16: 32,498,162-33,812,658	IGHV3OR16-12, IGHV3OR16-8, 36 more genes
nsv6622360	copy number variation	81	nstd224	human		GRCh37 chr14: 20,198,662-20,416,499 , GRCh38.p12 chr14: 19,730,503-19,948,340	OR4K6P, OR4K5, 11 more genes

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OSC8170 AND nstd224 (11)
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