1-0658-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4369824	copy number variation	1	nstd173	human		GRCh37 chr14: 41,563,049-41,585,724 , GRCh38.p12 chr14: 41,093,844-41,116,519	LINC02315
nsv4382371	copy number variation	1	nstd173	human		GRCh37 chrX: 82,885,451-83,020,628 , GRCh38.p12 chrX: 83,630,443-83,765,620	TERF1P4
nsv4379366	copy number variation	1	nstd173	human		GRCh37 chr10: 37,448,929-37,479,230 , GRCh38.p12 chr10: 37,160,001-37,190,302	ANKRD30A
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4383929	copy number variation	6	nstd173	human		GRCh37 chr14: 86,460,977-86,487,665 , GRCh38.p12 chr14: 85,994,633-86,021,321	LINC02328, LINC02316
nsv4368257	copy number variation	154	nstd173	human		GRCh37 chr11: 55,374,147-55,453,008 , GRCh38.p12 chr11: 55,606,671-55,685,532	OR4V1P, OR4P1P, 3 more genes
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4372893	copy number variation	16	nstd173	human		GRCh37 chr10: 47,588,964-47,692,945 , GRCh38.p12 chr10: 46,217,728-46,321,709	LOC105378577, AHCYP1, 2 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4379842	copy number variation	32	nstd173	human		GRCh37 chr14: 106,525,299-106,705,896 , GRCh38.p12 chr14: 106,069,054-106,249,305 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	LOC102724977, IGHV3-65, 113 more genes
nsv4381227	copy number variation	3	nstd173	human		GRCh37 chr14: 22,533,752-22,971,360 , GRCh38.p12 chr14: 22,065,488-22,502,376	TRAV41, TRDJ3, 63 more genes
nsv4377179	copy number variation	143	nstd173	human		GRCh37 chr3: 162,521,297-162,626,676 , GRCh38.p12 chr3: 162,803,509-162,908,888	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-0658-003 AND nstd173 (15)
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)