210240 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
nsv4387797	copy number variation	78	nstd173	human		GRCh37 chr1: 72,773,260-72,812,440 , GRCh38.p12 chr1: 72,307,577-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-67,982	LOC105378797
nsv4370970	copy number variation	2	nstd173	human		GRCh37 chr6: 320,859-381,137 , GRCh38.p12 chr6: 320,859-381,137	DUSP22
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4376437	copy number variation	46	nstd173	human		GRCh37 chr12: 11,503,156-11,553,849 , GRCh38.p12 chr12: 11,350,222-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,185-572,349	PRB1, PRB2
nsv4367142	copy number variation	135	nstd173	human		GRCh37 chr12: 2,235,941-2,259,954 , GRCh38.p12 chr12: 2,126,775-2,150,788 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-492,932	LOC107984131, CACNA1C
nsv4376724	copy number variation	112	nstd173	human		GRCh37 chr8: 39,246,772-39,397,015 , GRCh38.p12 chr8: 39,389,253-39,539,496	ADAM5, ADAM3A
nsv4369602	copy number variation	1	nstd173	human		GRCh37 chr8: 130,792,203-130,852,228 , GRCh38.p12 chr8: 129,779,957-129,839,982 , GRCh38.p12 chr8\|NW_019805494.1: 64,330-103,072	CYRIB, GSDMC
nsv4384996	copy number variation	2	nstd173	human		GRCh37 chrY: 25,415,736-25,609,620 , GRCh38.p12 chrY: 23,269,589-23,463,473	PPP1R12BP2, REREP1Y, 2 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
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4378235	copy number variation	17	nstd173	human		GRCh37 chr5: 180,378,776-180,430,789 , GRCh38.p12 chr5: 180,951,776-181,003,789	TMEM69P2, LOC100128762, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4380701	copy number variation	12	nstd173	human		GRCh37 chrY: 25,844,786-26,158,899 , GRCh38.p12 chrY: 23,698,639-24,012,752	RNU1-97P, USP9YP13, 18 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4368229	copy number variation	1	nstd173	human		GRCh37 chr22: 18,649,190-19,024,659 , GRCh38.p12 chr22: 18,166,423-19,037,146	POM121L15P, GGTLC3, 31 more genes
nsv4382819	copy number variation	1	nstd173	human		GRCh37 chr14: 22,441,153-22,970,223 , GRCh38.p12 chr14: 21,972,924-22,501,239	TRAV35, TRAJ39, 70 more genes
nsv4378591	copy number variation	3	nstd173	human		GRCh37 chr7: 142,226,368-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 622,348-808,802	PRSS3P1, WBP1LP1, 24 more genes
nsv4367958	copy number variation	71	nstd173	human		GRCh37 chr7: 38,293,950-38,378,483 , GRCh38.p12 chr7: 38,254,349-38,338,882	TRG, TRGV11, 15 more genes
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

210240 AND nstd173 (20)
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)