1-0722-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 15

loading data ...

Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4370464	copy number variation	362	nstd173	human		GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830	OR51A4, OR51A2
nsv4387280	copy number variation	24	nstd173	human		GRCh37 chr17: 44,213,649-44,292,754 , GRCh38.p12 chr17: 46,136,283-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 838,389-917,561	LOC107985027, KANSL1, 1 more genes
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4379867	copy number variation	5	nstd173	human		GRCh37 chr12: 11,220,827-11,241,337 , GRCh38.p12 chr12: 11,068,228-11,088,738	TAS2R64P, PRH1-TAS2R14, 2 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
nsv4386454	copy number variation	1	nstd173	human		GRCh37 chr13: 57,704,050-57,813,762 , GRCh38.p12 chr13: 57,129,916-57,239,628	PRR20A, PRR20B, 6 more genes
nsv4382222	copy number variation	125	nstd173	human		GRCh37 chr1: 248,688,587-248,795,289 , GRCh38.p12 chr1: 248,525,286-248,631,988	OR2AS1P, OR2T34, 4 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
nsv4369016	copy number variation	1	nstd173	human		GRCh37 chr7: 113,139,867-113,188,449 , GRCh38.p12 chr7: 113,499,812-113,548,394	0
nsv4374133	copy number variation	39	nstd173	human		GRCh37 chr3: 175,883,703-175,916,315 , GRCh38.p12 chr3: 176,165,915-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 50,426-83,038	0
nsv4377268	copy number variation	1	nstd173	human		GRCh37 chr10: 27,926,603-27,951,311 , GRCh38.p12 chr10: 27,637,674-27,662,382	0
nsv4375393	copy number variation	59	nstd173	human		GRCh37 chr17: 36,283,807-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 2,162,872-2,289,624	NPEPPSP1, TBC1D3, 6 more genes
nsv4372486	copy number variation	1	nstd173	human		GRCh37 chr14: 22,663,655-22,959,555 , GRCh38.p12 chr14: 22,195,761-22,490,567	TRAJ59, TRDJ4, 38 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-0722-003 AND nstd173 (16)
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)