2-1512-001 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
nsv4376284	copy number variation	379	nstd173	human		GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4384133	copy number variation	106	nstd173	human		GRCh37 chr1: 169,216,044-169,241,765 , GRCh38.p12 chr1: 169,246,806-169,272,527	NME7
nsv4366678	copy number variation	1	nstd173	human		GRCh37 chr10: 19,516,264-19,539,843 , GRCh38.p12 chr10: 19,227,335-19,250,914	MALRD1
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
nsv4372832	copy number variation	1	nstd173	human		GRCh37 chr7: 96,887,608-96,920,676 , GRCh38.p12 chr7: 97,258,296-97,291,364	LOC107986826
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
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
nsv4374916	copy number variation	1	nstd173	human		GRCh37 chr17: 44,201,425-44,292,754 , GRCh38.p12 chr17: 46,124,059-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 826,156-917,561	LOC107985027, KANSL1, 1 more genes
nsv4367386	copy number variation	50	nstd173	human		GRCh37 chr6: 257,061-294,826 , GRCh38.p12 chr6: 257,061-294,826	, DUSP22, 1 more genes
nsv4381422	copy number variation	10	nstd173	human		GRCh37 chr7: 155,056,383-155,082,078 , GRCh38.p12 chr7: 155,264,673-155,290,368	LOC105375589, LOC105375588, 1 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
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
nsv4378184	copy number variation	6	nstd173	human		GRCh37 chrX: 103,260,915-103,305,297 , GRCh38.p12 chrX: 104,006,343-104,050,731	LOC107985662, H2BW2, 1 more genes
nsv4383948	copy number variation	6	nstd173	human		GRCh37 chrX: 781,139-837,407 , GRCh38.p12 chrX: 820,404-876,672	0
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
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
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

2-1512-001 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)