11-0016-004 AND nstd173 - dbVar - NCBI

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

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4368058	copy number variation	90	nstd173	human		GRCh37 chr5: 97,043,561-97,093,733 , GRCh38.p12 chr5: 97,707,857-97,758,029	LOC391813
nsv4367129	copy number variation	8	nstd173	human		GRCh37 chr11: 49,710,704-49,760,797 , GRCh38.p12 chr11: 49,689,152-49,739,245 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-203,394	GRM5P1
nsv4378066	copy number variation	32	nstd173	human		GRCh37 chr19: 43,804,762-43,846,282 , GRCh38.p12 chr19: 43,300,610-43,342,130	CEACAMP4
nsv4379349	copy number variation	357	nstd173	human		GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351	SIRPB1
nsv4385917	copy number variation	155	nstd173	human		GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4384654	copy number variation	1	nstd173	human		GRCh37 chr5: 13,964,588-14,093,389 , GRCh38.p12 chr5: 13,964,479-14,093,280	DNAH5
nsv4376401	copy number variation	1	nstd173	human		GRCh37 chrX: 115,045,653-115,067,893 , GRCh38.p12 chrX: 115,929,320-115,951,560	DANT2
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4386054	copy number variation	20	nstd173	human		GRCh37 chr11: 55,374,176-55,442,305 , GRCh38.p12 chr11: 55,606,700-55,674,829	OR4S2, OR4C6, 2 more genes
nsv4383855	copy number variation	44	nstd173	human		GRCh37 chrX: 103,259,181-103,312,921 , GRCh38.p12 chrX: 104,004,609-104,058,356	H2BW2, LOC107985662, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4380669	copy number variation	1	nstd173	human		GRCh37 chr1: 1,627,906-1,687,675 , GRCh38.p12 chr1: 1,696,467-1,756,236	MMP23A, SLC35E2A, 4 more genes
nsv4380971	copy number variation	213	nstd173	human		GRCh37 chr6: 29,841,021-29,936,041 , GRCh38.p12 chr6: 29,873,244-29,968,264	HLA-H, HCG4P4, 12 more genes
nsv4370779	copy number variation	156	nstd173	human		GRCh37 chr5: 8,702,522-8,750,244 , GRCh38.p12 chr5: 8,702,410-8,750,132	0
nsv4367492	copy number variation	84	nstd173	human		GRCh37 chr4: 161,041,291-161,080,636 , GRCh38.p12 chr4: 160,120,139-160,159,484	0
nsv4372557	copy number variation	42	nstd173	human		GRCh37 chr6: 31,283,853-31,305,152 , GRCh38.p12 chr6: 31,316,076-31,337,375	0
nsv4382575	copy number variation	2	nstd173	human		GRCh37 chr21: 15,006,458-48,097,372 , GRCh38.p12 chr21: 13,634,137-46,677,460	CBR3-AS1, HSPA13, 639 more genes
nsv4384206	copy number variation	78	nstd173	human		GRCh37 chr5: 57,326,267-57,351,813 , GRCh38.p12 chr5: 58,030,440-58,055,986	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

11-0016-004 AND nstd173 (20)
dbVar
SAMN11080746 (1)
SRA

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)