OSC6766 AND nstd224 - dbVar - NCBI

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

Search results

Items: 10

loading data ...

Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6631779	copy number variation	63	nstd224	human		GRCh37 chr7: 141,772,099-141,794,376 , GRCh38.p12 chr7: 142,072,299-142,094,576 , GRCh38.p12 chr7\|NT_187562.1: 34,179-56,456	MGAM
nsv6630549	copy number variation	1	nstd224	human		GRCh37 chr5: 151,771,838-151,784,206 , GRCh38.p12 chr5: 152,392,277-152,404,645	NMUR2
nsv6628094	copy number variation	1	nstd224	human		GRCh37 chr2: 26,507-112,496 , GRCh38.p12 chr2: 26,507-112,496	FAM110C
nsv6624961	copy number variation	4	nstd224	human		GRCh37 chr19: 41,355,925-41,387,646 , GRCh38.p12 chr19: 40,850,020-40,881,741	CYP2A6, CYP2A7
nsv6622875	copy number variation	3	nstd224	human		GRCh37 chr15: 30,940,102-31,083,960 , GRCh38.p12 chr15: 30,647,899-30,791,757 , GRCh38.p12 chr15\|NT_187660.1: 2,933,433-3,077,466 , GRCh38.p12 chr15\|NW_011332701.1: 2,820,981-2,965,014	ARHGAP11B, LOC100288637
nsv6626928	copy number variation	93	nstd224	human		GRCh37 chr22: 24,374,253-24,386,612 , GRCh38.p12 chr22\|NT_187633.1: 268,428-280,787	GSTT1-AS1, GSTTP2, 2 more genes
nsv6629982	copy number variation	1	nstd224	human		GRCh37 chr4: 73,071-124,638 , GRCh38.p12 chr4: 73,179-124,756	ZNF595, ZNF718, 1 more genes
nsv6627098	copy number variation	2	nstd224	human		GRCh37 chr22: 33,462,254-33,473,566 , GRCh38.p12 chr22: 33,066,268-33,077,580	0
nsv6624084	copy number variation	158	nstd224	human		GRCh37 chr17: 44,179,983-44,353,222 , GRCh38.p12 chr17: 46,102,617-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 804,722-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6626622	copy number variation	14	nstd224	human		GRCh37 chr21: 15,235,277-15,263,760 , GRCh38.p12 chr21: 13,862,956-13,891,439	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

OSC6766 AND nstd224 (11)
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)