OSC5913 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
nsv6632493	copy number variation	72	nstd224	human		GRCh37 chr8: 137,688,230-137,855,721 , GRCh38.p12 chr8: 136,675,987-136,843,478	LINC02055
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
nsv6624315	copy number variation	13	nstd224	human		GRCh37 chr17: 77,368,568-77,390,725 , GRCh38.p12 chr17: 79,372,486-79,394,643	RBFOX3
nsv6631843	copy number variation	45	nstd224	human		GRCh37 chr7: 142,835,239-142,881,540 , GRCh38.p12 chr7: 143,138,146-143,184,447	PIP, TAS2R39
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 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
nsv6628246	copy number variation	29	nstd224	human		GRCh37 chr3: 100,355,338-100,441,859 , GRCh38.p12 chr3: 100,636,494-100,723,015	TFG, ADGRG7, 1 more genes
nsv6625676	copy number variation	58	nstd224	human		GRCh37 chr1: 17,211,616-17,265,416 , GRCh38.p12 chr1: 16,885,121-16,938,921	LOC107985101, TRN-GTT4-1, 3 more genes
nsv6624231	copy number variation	76	nstd224	human		GRCh37 chr17: 34,438,753-34,476,927 , GRCh38.p12 chr17: 36,111,360-36,149,545 , GRCh38.p12 chr17\|NT_187661.1: 65,457-103,642 , GRCh38.p12 chr17\|NT_187614.1: 346,281-384,455	LOC107985055, LOC101927369, 1 more genes
nsv6633913	copy number variation	15	nstd224	human		GRCh37 chr9: 43,393,590-43,428,145 , GRCh38.p12 chr9: 42,383,725-42,418,560	ATP5F1AP1, FKBP4P6, 1 more genes
nsv6623452	copy number variation	77	nstd224	human		GRCh37 chr16: 32,480,049-33,772,866 , GRCh38.p12 chr16: 32,468,728-33,970,399	ABCD1P3, IGHV3OR16-7, 44 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
nsv6622002	copy number variation	111	nstd224	human		GRCh37 chr14: 20,198,662-20,417,653 , GRCh38.p12 chr14: 19,730,503-19,949,494	OR4N1P, OR4K3, 11 more genes
nsv6633894	copy number variation	1	nstd224	human		GRCh37 chr9: 29,236,498-29,315,660 , GRCh38.p12 chr9: 29,236,500-29,315,662	0
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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