OSC6196 AND nstd224 - dbVar - NCBI

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Items: 11

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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
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
nsv6633457	copy number variation	1	nstd224	human		GRCh37 chr9: 4,337,191-4,462,265 , GRCh38.p12 chr9: 4,337,191-4,462,265	RNU6-694P
nsv6632229	copy number variation	1	nstd224	human		GRCh37 chr7: 98,759,117-98,805,706 , GRCh38.p12 chr7: 99,161,494-99,208,083 , GRCh38.p12 chr7\|NW_017852929.1: 69,123-115,712	KPNA7
nsv6623118	copy number variation	1	nstd224	human		GRCh37 chr15: 46,216,043-46,431,777 , GRCh38.p12 chr15: 45,923,845-46,139,579	LOC100419366, LOC105370802
nsv6628599	copy number variation	1	nstd224	human		GRCh37 chr3: 4,074,425-4,159,879 , GRCh38.p12 chr3: 4,032,741-4,118,195	SUMF1, LOC102723512
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
nsv6625607	copy number variation	17	nstd224	human		GRCh37 chr1: 12,865,657-12,948,317 , GRCh38.p12 chr1: 12,805,521-12,888,493	PRAMEF2, HNRNPCL1, 4 more genes
nsv6623654	copy number variation	84	nstd224	human		GRCh37 chr16: 32,509,483-33,772,866 , GRCh38.p12 chr16: 32,498,162-33,970,399	IGHV3OR16-11, LOC342443, 43 more genes
nsv6633451	copy number variation	13	nstd224	human		GRCh37 chr9: 32,105,254-32,122,888 , GRCh38.p12 chr9: 32,105,256-32,122,890	0
nsv6622245	copy number variation	46	nstd224	human		GRCh37 chr14: 20,220,501-20,416,499 , GRCh38.p12 chr14: 19,752,342-19,948,340	OR4K6P, OR4K5, 10 more genes
nsv6627080	copy number variation	26	nstd224	human		GRCh37 chr22: 24,302,487-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,662-284,607	GSTT1, DDTL, 10 more genes

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OSC6196 AND nstd224 (12)
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