OSC3194 AND nstd224 - dbVar - NCBI

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

Search results

Items: 11

loading data ...

Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6628914	copy number variation	179	nstd224	human		GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491	NLGN1
nsv6626656	copy number variation	2	nstd224	human		GRCh37 chr21: 47,821,583-47,831,667 , GRCh38.p12 chr21: 46,401,669-46,411,753	PCNT
nsv6624132	copy number variation	8	nstd224	human		GRCh37 chr18: 13,731,520-13,741,519 , GRCh38.p12 chr18: 13,731,521-13,741,520	RNMT
nsv6632687	copy number variation	8	nstd224	human		GRCh37 chr8: 144,943,389-144,999,874 , GRCh38.p12 chr8: 143,869,221-143,925,706	EPPK1, PLEC
nsv6634030	copy number variation	1	nstd224	human		GRCh37 chr9: 98,678,657-98,703,768 , GRCh38.p12 chr9: 95,916,375-95,941,486	PARK7P2, ERCC6L2
nsv6620184	copy number variation	5	nstd224	human		GRCh37 chr10: 135,013,923-135,032,385 , GRCh38.p12 chr10: 133,200,419-133,218,881	LOC105378573, KNDC1
nsv6633226	copy number variation	78	nstd224	human		GRCh37 chr9: 140,166,981-140,196,334 , GRCh38.p12 chr9: 137,272,529-137,301,882	NRARP, TOR4A, 1 more genes
nsv6625598	copy number variation	2	nstd224	human		GRCh37 chr1: 1,216,848-1,244,646 , GRCh38.p12 chr1: 1,281,468-1,309,266	SCNN1D, PUSL1, 3 more genes
nsv6634221	copy number variation	1	nstd224	human		GRCh37 chrX: 140,559,503-140,779,598 , GRCh38.p12 chrX: 141,471,509-141,691,441	SPANXA1, SPANXA2-OT1, 2 more genes
nsv6621849	copy number variation	162	nstd224	human		GRCh37 chr12: 8,003,758-8,123,306 , GRCh38.p12 chr12: 7,851,162-7,970,710	SLC2A14, RPS20P29, 3 more genes
nsv6627146	copy number variation	1	nstd224	human		GRCh37 chr21: 29,201,063-29,361,630 , GRCh38.p12 chr21: 27,828,744-27,989,311	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC3194 AND nstd224 (12)
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)