10-0015-002 AND nstd173 - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 17

loading data ...

Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4378713	copy number variation	50	nstd173	human		GRCh37 chr5: 155,471,684-155,500,768 , GRCh38.p12 chr5: 156,044,674-156,073,758	SGCD
nsv4381717	copy number variation	19	nstd173	human		GRCh37 chr16: 55,796,376-55,816,692 , GRCh38.p12 chr16: 55,762,464-55,782,780	CES1P1
nsv4380279	copy number variation	2	nstd173	human		GRCh37 chr13: 57,758,269-57,789,575 , GRCh38.p12 chr13: 57,184,135-57,215,441	LOC105370216, MTCO2P3
nsv4383038	copy number variation	15	nstd173	human		GRCh37 chr5: 180,374,898-180,430,801 , GRCh38.p12 chr5: 180,947,898-181,003,801	BTNL8, ARPP19P1, 3 more genes
nsv4386149	copy number variation	1	nstd173	human		GRCh37 chr17: 4,098,261-4,210,279 , GRCh38.p12 chr17: 4,194,966-4,306,984	LOC100420060, MFSD1P1, 3 more genes
nsv4377612	copy number variation	1	nstd173	human		GRCh37 chr1: 226,254,078-226,354,550 , GRCh38.p12 chr1: 226,066,377-226,166,849	ACBD3, LOC112268255, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4381233	copy number variation	1	nstd173	human		GRCh37 chr4: 69,435,901-69,481,721 , GRCh38.p12 chr4: 68,570,183-68,616,003	LOC100132651, LOC100422402, 1 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4382222	copy number variation	125	nstd173	human		GRCh37 chr1: 248,688,587-248,795,289 , GRCh38.p12 chr1: 248,525,286-248,631,988	OR2AS1P, OR2T34, 4 more genes
nsv4366642	copy number variation	8	nstd173	human		GRCh37 chr14: 106,536,991-106,849,677 , GRCh38.p12 chr14: 106,112,755-106,393,766 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGHVIII-67-3, LINC00226, 113 more genes
nsv4376368	copy number variation	168	nstd173	human		GRCh37 chr6: 67,009,023-67,048,629 , GRCh38.p12 chr6: 66,299,130-66,338,736	0
nsv4374799	copy number variation	11	nstd173	human		GRCh37 chr10: 46,966,534-47,688,677 , GRCh38.p12 chr10: 46,157,935-47,923,579	FAM25BP, RN7SL248P, 54 more genes
nsv4366041	copy number variation	13	nstd173	human		GRCh37 chr14: 22,462,737-22,974,280 , GRCh38.p12 chr14: 21,994,497-22,505,293	TRAV29DV5, TRAJ48, 71 more genes
nsv4366133	copy number variation	16	nstd173	human		GRCh37 chr7: 142,246,905-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBJ1-1, TRBV24-1, 23 more genes
nsv4369622	copy number variation	14	nstd173	human		GRCh37 chr7: 38,294,088-38,391,352 , GRCh38.p12 chr7: 38,254,487-38,351,751	TRGV11, TRG, 19 more genes
nsv4368473	copy number variation	289	nstd173	human		GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

10-0015-002 AND nstd173 (18)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)