MS20854 AND nstd71 - dbVar - NCBI

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

Search results

Items: 12

loading data ...

Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898508	copy number variation	27	nstd71	human		NCBI36 chr11: 133,859,037-133,984,501 , GRCh37.p13 chr11: 134,353,827-134,479,291 , GRCh38.p12 chr11: 134,483,933-134,609,397	B3GAT1-DT
nsv883743	copy number variation	17	nstd71	human		NCBI36 chr6: 29,972,294-29,992,625 , GRCh37.p13 chr6: 29,864,315-29,884,646 , GRCh37.p13 chr6\|NT_167246.1: 1,158,492-1,178,821 , GRCh38.p12 chr6: 29,896,538-29,916,869 , GRCh38.p12 chr6\|NT_167246.2: 1,152,872-1,173,201	DDX39BP1, HLA-T, 3 more genes
nsv874807	copy number variation	39	nstd71	human		NCBI36 chr2: 110,201,336-111,021,091 , GRCh37.p13 chr2: 110,844,047-111,334,482 , GRCh38.p12 chr2: 110,086,470-110,576,877	ZBTB45P2, RGPD6, 17 more genes
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv891346	copy number variation	3	nstd71	human		NCBI36 chr8: 115,052,464-115,096,852 , GRCh37.p13 chr8: 114,983,288-115,027,676 , GRCh38.p12 chr8: 113,971,059-114,015,447	0
nsv882605	copy number variation	7	nstd71	human		NCBI36 chr5: 104,532,646-104,576,058 , GRCh37.p13 chr5: 104,504,747-104,548,159 , GRCh38.p12 chr5: 105,169,046-105,212,458	0
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
nsv884262	copy number variation	7	nstd71	human		NCBI36 chr6: 31,388,306-31,403,505 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,629,243 , GRCh37.p13 chr6: 31,280,327-31,295,526 , GRCh38.p12 chr6: 31,312,550-31,327,749 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,629,945	0
nsv886198	copy number variation	304	nstd71	human		NCBI36 chr6: 77,073,066-77,088,077 , GRCh37.p13 chr6: 77,016,346-77,031,357 , GRCh38.p12 chr6: 76,306,629-76,321,640	0
nsv881753	copy number variation	1	nstd71	human		NCBI36 chr5: 63,900,153-64,545,463 , GRCh37.p13 chr5: 63,864,397-64,509,707 , GRCh38.p12 chr5: 64,568,570-65,213,880	ADAMTS6, SREK1IP1, 7 more genes
nsv896363	copy number variation	13	nstd71	human		NCBI36 chr10: 135,106,317-135,252,190 , GRCh37.p13 chr10: 135,256,327-135,402,200 , GRCh38.p12 chr10: 133,442,823-133,588,696	CYP2E1, LOC105378575, 7 more genes
nsv893209	copy number variation	57	nstd71	human		NCBI36 chr9: 43,532,092-44,683,090 , GRCh37.p13 chr9: 43,592,096-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	FAM74A7, CNTNAP3B, 30 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS20854 AND nstd71 (13)
dbVar
MS11738 AND nstd71 (9)
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)