OSC8573 AND nstd224 - dbVar - NCBI

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Items: 10

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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
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
nsv6633974	copy number variation	6	nstd224	human		GRCh37 chr9: 28,595,171-28,759,813 , GRCh38.p12 chr9: 28,595,173-28,759,815	LINGO2, LOC105376003, 2 more genes
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6626929	copy number variation	17	nstd224	human		GRCh37 chr22: 24,374,672-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,847-284,607	GSTT1-AS1, GSTTP2, 1 more genes
nsv6629652	copy number variation	1	nstd224	human		GRCh37 chr4: 188,838,522-188,861,899 , GRCh38.p12 chr4: 187,917,368-187,940,745	0
nsv6626995	copy number variation	1	nstd224	human		GRCh37 chr21: 25,748,456-25,758,848 , GRCh38.p12 chr21: 24,376,142-24,386,534	0
nsv6620628	copy number variation	93	nstd224	human		GRCh37 chr10: 47,146,867-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,739,149	GDF10, RBP3, 48 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
nsv6627895	copy number variation	12	nstd224	human		GRCh37 chr2: 57,402,202-57,455,549 , GRCh38.p12 chr2: 57,175,067-57,228,414	0

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OSC8573 AND nstd224 (11)
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