OSC6114 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
nsv6632584	copy number variation	3	nstd224	human		GRCh37 chr8: 15,950,391-16,021,468 , GRCh38.p12 chr8: 16,092,882-16,163,959	MSR1
nsv6630897	copy number variation	21	nstd224	human		GRCh37 chr5: 97,051,856-97,096,543 , GRCh38.p12 chr5: 97,716,152-97,760,839	LOC391813
nsv6631634	copy number variation	1	nstd224	human		GRCh37 chr7: 141,772,099-141,782,969 , GRCh38.p12 chr7: 142,072,299-142,083,169 , GRCh38.p12 chr7\|NT_187562.1: 34,179-45,049	MGAM
nsv6632960	copy number variation	13	nstd224	human		GRCh37 chr8: 2,132,549-2,178,550 , GRCh38.p12 chr8: 2,184,352-2,230,882 , GRCh38.p12 chr8\|NT_187576.1: 367,759-413,760	LOC105377782, LOC105377781
nsv6632968	copy number variation	4	nstd224	human		GRCh37 chr8: 2,342,334-2,585,105 , GRCh38.p12 chr8: 2,605,460-2,727,565 , GRCh38.p12 chr8\|NT_187576.1: 652,904-809,178	LINC03021, LOC107986865
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
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
nsv6631991	copy number variation	2	nstd224	human		GRCh37 chr7: 70,317,727-70,363,019 , GRCh38.p12 chr7: 70,852,741-70,898,033	0

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