15-1132-002 AND nstd173 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4377582	copy number variation	1	nstd173	human		GRCh37 chr20: 14,377,968-14,415,228 , GRCh38.p12 chr20: 14,397,322-14,434,582	MACROD2
nsv4382054	copy number variation	13	nstd173	human		GRCh37 chr6: 55,825,495-55,852,141 , GRCh38.p12 chr6: 55,960,697-55,987,343	LOC107986539
nsv4377460	copy number variation	116	nstd173	human		GRCh37 chr16: 60,553,311-60,575,074 , GRCh38.p12 chr16: 60,519,407-60,541,170	LOC101927605
nsv4373295	copy number variation	124	nstd173	human		GRCh37 chr13: 69,248,299-69,268,719 , GRCh38.p12 chr13: 68,674,167-68,694,587	RN7SL761P
nsv4372210	copy number variation	1	nstd173	human		GRCh37 chr19: 49,023,610-49,097,887 , GRCh38.p12 chr19: 48,520,353-48,594,630	SULT2B1
nsv4366472	copy number variation	183	nstd173	human		GRCh37 chr3: 46,793,072-46,849,588 , GRCh38.p12 chr3: 46,751,582-46,808,098	PRSS44P, PRSS43P
nsv4367045	copy number variation	1	nstd173	human		GRCh37 chr15: 55,527,874-55,621,439 , GRCh38.p12 chr15: 55,235,676-55,329,241	RAB27A, PIGB, 1 more genes
nsv4366556	copy number variation	72	nstd173	human		GRCh37 chr6: 254,254-294,826 , GRCh38.p12 chr6: 254,254-294,826	DUSP22, , 1 more genes
nsv4375662	copy number variation	272	nstd173	human		GRCh37 chr11: 5,783,910-5,809,230 , GRCh38.p12 chr11: 5,762,680-5,788,000	OR52N1, OR56B2P, 1 more genes
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
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4381194	copy number variation	2	nstd173	human		GRCh37 chr7: 38,319,296-38,351,975 , GRCh38.p12 chr7: 38,279,695-38,312,374	LOC103689914, TRGV11, 4 more genes
nsv4365433	copy number variation	1	nstd173	human		GRCh37 chr17: 62,621,680-62,974,197 , GRCh38.p12 chr17: 64,625,562-64,978,079	LOC102929163, SLC16A6P1, 17 more genes
nsv4386998	copy number variation	1	nstd173	human		GRCh37 chr2: 82,196,769-82,319,437 , GRCh38.p12 chr2: 81,969,645-82,092,313	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

15-1132-002 AND nstd173 (15)
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)