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

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)