1-0139-001 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
nsv4375641	copy number variation	3	nstd173	human		GRCh37 chrX: 32,999,487-33,020,261 , GRCh38.p12 chrX: 32,981,370-33,002,144	DMD
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
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
nsv4365651	copy number variation	1	nstd173	human		GRCh37 chr3: 87,948,318-88,007,774 , GRCh38.p12 chr3: 87,899,168-87,958,624	HTR1F, RNU6ATAC6P
nsv4383205	copy number variation	42	nstd173	human		GRCh37 chr12: 11,220,827-11,247,388 , GRCh38.p12 chr12: 11,068,228-11,094,789	PRH1-PRR4, PRH1-TAS2R14, 3 more genes
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4367860	copy number variation	6	nstd173	human		GRCh37 chr19: 42,259,136-42,305,800 , GRCh38.p12 chr19: 41,755,228-41,801,868	CEACAM6, LOC112268252, 1 more genes
nsv4381838	copy number variation	5	nstd173	human		GRCh37 chr19: 54,722,728-54,753,327 , GRCh38.p12 chr19: 54,218,859-54,249,469 , GRCh38.p12 chr19\|NT_187693.1: 193,842-224,441 , GRCh38.p12 chr19\|NW_003571061.2: 193,842-224,473 , GRCh38.p12 chr19\|NW_003571060.1: 193,845-224,437 , GRCh38.p12 chr19\|NW_003571054.1: 193,659-224,204	LILRB5, LILRB3, 7 more genes
nsv4366417	copy number variation	1	nstd173	human		GRCh37 chr4: 36,914,433-36,949,710 , GRCh38.p12 chr4: 36,912,811-36,948,088	0
nsv4373135	copy number variation	6	nstd173	human		GRCh37 chrX: 154,385,633-154,417,811 , GRCh38.p12 chrX: 155,157,358-155,189,536	0
nsv4380626	copy number variation	21	nstd173	human		GRCh37 chr3: 175,888,455-175,916,315 , GRCh38.p12 chr3: 176,170,667-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 55,178-83,038	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4388179	copy number variation	3	nstd173	human		GRCh37 chr22: 22,311,349-22,573,197 , GRCh38.p12 chr22: 21,956,977-22,218,805	IGLVI-56, IGLVV-58, 26 more genes
nsv4370664	copy number variation	5	nstd173	human		GRCh37 chr14: 22,761,289-22,944,507 , GRCh38.p12 chr14: 22,293,404-22,475,517	TRAJ60, TRDC, 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
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-0139-001 AND nstd173 (18)
dbVar
SRA for PMC (Select 3688379) (12)
SRA

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)