199597 AND nstd173 - dbVar - NCBI

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

Search results

Items: 18

loading data ...

Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4373762	copy number variation	73	nstd173	human		GRCh37 chr6: 55,823,233-55,852,141 , GRCh38.p12 chr6: 55,958,435-55,987,343	LOC107986539
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4371021	copy number variation	9	nstd173	human		GRCh37 chr8: 15,402,856-15,423,270 , GRCh38.p12 chr8: 15,545,347-15,565,761	TUSC3
nsv4379155	copy number variation	63	nstd173	human		GRCh37 chr3: 173,239,853-173,289,847 , GRCh38.p12 chr3: 173,522,063-173,572,057	NLGN1
nsv4374158	copy number variation	106	nstd173	human		GRCh37 chr3: 128,380,595-128,412,365 , GRCh38.p12 chr3: 128,661,752-128,693,522	POU5F1P6
nsv4383676	copy number variation	3	nstd173	human		GRCh37 chr11: 55,374,019-55,422,251 , GRCh38.p12 chr11: 55,606,543-55,654,775	OR4P4, OR4S2
nsv4366793	copy number variation	39	nstd173	human		GRCh37 chr6: 254,254-381,137 , GRCh38.p12 chr6: 254,254-381,137	, DUSP22, 1 more genes
nsv4384776	copy number variation	87	nstd173	human		GRCh37 chr19: 52,131,800-52,154,905 , GRCh38.p12 chr19: 51,628,547-51,651,652	SIGLEC5, SIGLEC14, 1 more genes
nsv4381902	copy number variation	86	nstd173	human		GRCh37 chr17: 44,187,492-44,292,754 , GRCh38.p12 chr17: 46,110,126-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 812,225-917,561	LOC107985027, KANSL1-AS1, 1 more genes
nsv4385137	copy number variation	28	nstd173	human		GRCh37 chr5: 180,374,484-180,430,789 , GRCh38.p12 chr5: 180,947,484-181,003,789	TMEM69P2, LOC100128762, 3 more genes
nsv4375644	copy number variation	145	nstd173	human		GRCh37 chr22: 25,656,238-25,922,334 , GRCh38.p12 chr22: 25,260,271-25,526,367	CRYBB2P1, IGLL3P, 4 more genes
nsv4369166	copy number variation	31	nstd173	human		GRCh37 chr8: 13,611,631-13,652,975 , GRCh38.p12 chr8: 13,754,122-13,795,466	0
nsv4381531	copy number variation	237	nstd173	human		GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4368350	copy number variation	114	nstd173	human		GRCh37 chr17: 34,425,363-34,477,480 , GRCh38.p12 chr17: 36,097,969-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 52,066-104,195 , GRCh38.p12 chr17\|NT_187614.1: 332,891-385,008	CCL4, LOC101927369, 4 more genes
nsv4365131	copy number variation	54	nstd173	human		GRCh37 chr14: 22,404,167-22,974,280 , GRCh38.p12 chr14: 21,935,993-22,505,293	TRAJ46, TRAJ57, 76 more genes
nsv4370415	copy number variation	102	nstd173	human		GRCh37 chr7: 38,294,983-38,394,857 , GRCh38.p12 chr7: 38,255,382-38,355,256	TRGV5, TRGV7, 19 more genes
nsv4373308	copy number variation	84	nstd173	human		GRCh37 chr14: 106,525,299-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

199597 AND nstd173 (19)
dbVar
ClinVar for MedGen (Select 355454) (1011)
ClinVar
Nucleotide Links for Protein (Select 1370509635) (2)
Nucleotide

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)