OSC6443 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6627352	copy number variation	3	nstd224	human		GRCh37 chr2: 153,670,186-153,797,204 , GRCh38.p12 chr2: 152,813,672-152,940,690	UBQLN4P2
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
nsv6629885	copy number variation	1	nstd224	human		GRCh37 chr4: 65,297,140-65,314,342 , GRCh38.p12 chr4: 64,431,422-64,448,624	DPP3P1
nsv6625538	copy number variation	421	nstd224	human		GRCh37 chr1: 110,228,436-110,241,385 , GRCh38.p12 chr1: 109,685,814-109,698,763	GSTM1
nsv6624552	copy number variation	1	nstd224	human		GRCh37 chr18: 3,362,029-3,424,358 , GRCh38.p12 chr18: 3,362,031-3,424,360	TGIF1, BOD1P1, 3 more genes
nsv6626372	copy number variation	1	nstd224	human		GRCh37 chr1: 26,527,163-26,561,369 , GRCh38.p12 chr1: 26,200,672-26,234,878	CATSPER4, CEP85, 2 more genes
nsv6627470	copy number variation	16	nstd224	human		GRCh37 chr22: 42,523,678-42,536,064 , GRCh38.p12 chr22\|NT_187682.1: 50,017-62,403	CYP2D6, CYP2D7, 1 more genes
nsv6625391	copy number variation	84	nstd224	human		GRCh37 chr1: 149,036,931-149,186,834 , GRCh38.p12 chr1: 143,542,264-143,692,183	NBPF17P, PFN1P12, 5 more genes
nsv6622145	copy number variation	1	nstd224	human		GRCh37 chr13: 43,478,867-43,769,344 , GRCh38.p12 chr13: 42,904,731-43,195,208	DNAJC15, EPSTI1, 5 more genes
nsv6627200	copy number variation	37	nstd224	human		GRCh37 chr22: 24,302,601-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,776-284,607	GSTT1, GSTT2B, 10 more genes
nsv6626851	copy number variation	60	nstd224	human		GRCh37 chr21: 15,248,281-15,263,760 , GRCh38.p12 chr21: 13,875,960-13,891,439	0

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OSC6443 AND nstd224 (12)
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