1-0639-004 AND nstd173 - dbVar - NCBI

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

Search results

Items: 16

loading data ...

Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4370607	copy number variation	1	nstd173	human		GRCh37 chr13: 82,906,859-83,052,404 , GRCh38.p12 chr13: 82,332,724-82,478,269	LOC105370285
nsv4376284	copy number variation	379	nstd173	human		GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4375716	copy number variation	91	nstd173	human		GRCh37 chr3: 165,041,535-165,085,386 , GRCh38.p12 chr3: 165,323,747-165,367,598	LINC01322
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
nsv4377753	copy number variation	5	nstd173	human		GRCh37 chr8: 95,398,026-95,424,814 , GRCh38.p12 chr8: 94,385,798-94,412,586	RAD54B
nsv4380005	copy number variation	18	nstd173	human		GRCh37 chr11: 18,941,197-18,961,339 , GRCh38.p12 chr11: 18,919,650-18,939,792	MRGPRX1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4382503	copy number variation	75	nstd173	human		GRCh37 chr4: 69,367,105-69,485,978 , GRCh38.p12 chr4: 68,501,387-68,620,260	UGT2B29P, LOC100422402, 2 more genes
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4367386	copy number variation	50	nstd173	human		GRCh37 chr6: 257,061-294,826 , GRCh38.p12 chr6: 257,061-294,826	, DUSP22, 1 more genes
nsv4378626	copy number variation	12	nstd173	human		GRCh37 chr17: 44,212,362-44,292,754 , GRCh38.p12 chr17: 46,134,996-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,103-917,561	KANSL1-AS1, KANSL1, 1 more genes
nsv4371487	copy number variation	89	nstd173	human		GRCh37 chr19: 20,596,106-20,720,705 , GRCh38.p12 chr19: 20,413,300-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4378844	copy number variation	3	nstd173	human		GRCh37 chr6: 31,359,874-31,456,073 , GRCh38.p12 chr6: 31,392,097-31,488,296	HCP5, HLA-X, 5 more genes
nsv4383495	copy number variation	2	nstd173	human		GRCh37 chr6: 31,952,483-32,030,324 , GRCh38.p12 chr6: 31,984,706-32,062,547	C4A, C4B, 5 more genes
nsv4380539	copy number variation	3	nstd173	human		GRCh37 chr18: 58,100,320-58,121,041 , GRCh38.p12 chr18: 60,433,087-60,453,808	0
nsv4378485	copy number variation	15	nstd173	human		GRCh37 chr14: 22,752,693-22,959,555 , GRCh38.p12 chr14: 22,284,810-22,490,567	, TRDD3, 31 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

1-0639-004 AND nstd173 (17)
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)