OSC5852 AND nstd224 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6621752	copy number variation	10	nstd224	human		GRCh37 chr12: 83,168,827-83,206,342 , GRCh38.p12 chr12: 82,775,048-82,812,563	TMTC2
nsv6621764	copy number variation	15	nstd224	human		GRCh37 chr12: 99,994,957-100,008,409 , GRCh38.p12 chr12: 99,601,179-99,614,631	ANKS1B
nsv6630546	copy number variation	3	nstd224	human		GRCh37 chr5: 5,686,448-5,710,888 , GRCh38.p12 chr5: 5,686,335-5,710,775	LOC105374634
nsv6624576	copy number variation	9	nstd224	human		GRCh37 chr18: 1,906,066-1,977,713 , GRCh38.p12 chr18: 1,906,065-1,977,712	AIDAP3, LOC105371958
nsv6629641	copy number variation	1	nstd224	human		GRCh37 chr4: 184,622,936-184,641,445 , GRCh38.p12 chr4: 183,701,783-183,720,292	TRAPPC11, RNU6-1053P
nsv6624482	copy number variation	3	nstd224	human		GRCh37 chr19: 41,349,977-41,381,553 , GRCh38.p12 chr19: 40,844,072-40,875,648	CYP2A6, CYP2A7
nsv6621807	copy number variation	3	nstd224	human		GRCh37 chr12: 49,676,010-49,690,509 , GRCh38.p12 chr12: 49,282,227-49,296,726	TROAP-AS1, PRPH
nsv6623632	copy number variation	20	nstd224	human		GRCh37 chr16: 28,608,993-28,622,773 , GRCh38.p12 chr16: 28,597,672-28,611,452	LOC107984835, SULT1A1
nsv6629306	copy number variation	49	nstd224	human		GRCh37 chr3: 75,447,252-75,563,370 , GRCh38.p12 chr3: 75,398,101-75,514,219	LINC02018, FAM86DP, 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
nsv6620629	copy number variation	33	nstd224	human		GRCh37 chr10: 47,536,152-47,703,869 , GRCh38.p12 chr10: 46,164,916-46,332,633	ANTXRL, LOC105378577, 2 more genes
nsv6631082	copy number variation	194	nstd224	human		GRCh37 chr6: 67,017,494-67,044,618 , GRCh38.p12 chr6: 66,307,601-66,334,725	0
nsv6621781	copy number variation	84	nstd224	human		GRCh37 chr12: 31,266,287-31,402,690 , GRCh38.p12 chr12: 31,113,353-31,249,756 , GRCh38.p12 chr12\|NT_187587.1: 1,874-140,550	OVOS2, LOC101060058, 4 more genes
nsv6624073	copy number variation	6	nstd224	human		GRCh37 chr17: 33,682,734-33,766,040 , GRCh38.p12 chr17: 35,355,715-35,439,021	SLFN12, SLFN11, 4 more genes
nsv6623220	copy number variation	151	nstd224	human		GRCh37 chr16: 34,489,371-34,724,788 , GRCh38.p12 chr16: 35,255,000-35,490,417	AGGF1P4, C2orf69P3, 21 more genes

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