"nstd11"[study] AND "copy-neutral loss of heterozygosity"[variant_type - dbVar - NCBI

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

Search results

Items: 8

loading data ...

Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv429616	copy number variation	1	nstd11	human		NCBI36 chr13: 19,386,212-114,093,817 , GRCh37.p13 chr13: 20,488,212-115,075,715 , GRCh38.p12 chr13: 19,914,072-114,310,240	PARP4, PARP1P1, 1314 more genes
nsv429618	copy number variation	1	nstd11	human		NCBI36 chr13: 25,236,798-113,967,827 , GRCh37.p13 chr13: 26,338,798-114,949,725 , GRCh38.p12 chr13: 25,779,197-114,184,250	PARP1P1, ALOX5AP, 1174 more genes
nsv429615	copy number variation	1	nstd11	human		NCBI36 chr11: 196,767-49,155,500 , GRCh37.p13 chr11: 206,767-49,198,924 , GRCh38.p12 chr11: 206,767-49,177,372	ACP2, ADM, 976 more genes
nsv429559	copy number variation	1	nstd11	human		NCBI36 chr11: 211,584-48,203,033 , GRCh37.p13 chr11: 221,584-48,246,457 , GRCh38.p12 chr11: 221,584-48,224,905	ACP2, ADM, 938 more genes
nsv429550	copy number variation	1	nstd11	human		NCBI36 chr11: 214,676-43,781,942 , GRCh37.p13 chr11: 224,676-43,825,366 , GRCh38.p12 chr11: 224,676-43,803,816	ADM, AP2A2, 837 more genes
nsv429610	copy number variation	1	nstd11	human		NCBI36 chr6: 110,632-42,839,093 , GRCh37.p13 chr6: 165,632-42,731,115 , GRCh38.p12 chr6: 165,632-42,763,377	ABCF1, AGER, 1322 more genes
nsv429623	copy number variation	1	nstd11	human		NCBI36 chr16: 41,263-30,461,660 , GRCh37.p13 chr16: 101,263-30,554,159 , GRCh38.p12 chr16: 51,263-30,542,838	ABAT, ABCA3, 853 more genes
nsv429619	copy number variation	1	nstd11	human		NCBI36 chr16: 54,535-11,398,508 , GRCh37.p13 chr16: 114,535-11,491,007 , GRCh38.p12 chr16: 64,537-11,397,150	ABAT, ABCA3, 397 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

"nstd11"[study] AND "copy-neutral loss of heterozygosity"[variant... (9)
"nstd11"[study] AND "copy-neutral loss of heterozygosity"[variant_type]
Search

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)