2-1272-001 AND nstd173 - 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
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4378308	copy number variation	1	nstd173	human		GRCh37 chr9: 86,156,262-86,192,212 , GRCh38.p12 chr9: 83,541,347-83,577,297	FRMD3
nsv4369656	copy number variation	16	nstd173	human		GRCh37 chr5: 9,901,952-9,926,287 , GRCh38.p12 chr5: 9,901,840-9,926,175	LINC02112
nsv4383907	copy number variation	2	nstd173	human		GRCh37 chr2: 28,792,031-28,815,986 , GRCh38.p12 chr2: 28,569,164-28,593,119	PLB1
nsv4376614	copy number variation	1	nstd173	human		GRCh37 chr17: 15,513,003-15,546,790 , GRCh38.p12 chr17: 15,609,689-15,643,476	TRIM16, FBXW10B
nsv4370404	copy number variation	4	nstd173	human		GRCh37 chr9: 137,338,693-137,469,523 , GRCh38.p12 chr9: 134,446,847-134,577,677	LOC100506532, LOC105376311
nsv4385359	copy number variation	71	nstd173	human		GRCh37 chr12: 11,216,817-11,251,920 , GRCh38.p12 chr12: 11,064,218-11,099,321	PRH1, TAS2R64P, 3 more genes
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 more genes
nsv4368892	copy number variation	173	nstd173	human		GRCh37 chr14: 106,530,472-106,693,442 , GRCh38.p12 chr14: 106,074,229-106,236,829 , GRCh38.p12 chr14\|NT_187600.1: 541,998-704,598	LOC105370700, IGHV3-19, 19 more genes
nsv4369507	copy number variation	22	nstd173	human		GRCh37 chr6: 103,738,313-103,759,824 , GRCh38.p12 chr6: 103,290,438-103,311,949	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

2-1272-001 AND nstd173 (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)