1-0514-002 AND nstd173 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4368568	copy number variation	177	nstd173	human		GRCh37 chr14: 41,610,556-41,657,457 , GRCh38.p12 chr14: 41,141,353-41,188,254	LINC02315
nsv4380463	copy number variation	77	nstd173	human		GRCh37 chr2: 98,118,115-98,162,176 , GRCh38.p12 chr2: 97,501,652-97,545,713	ANKRD36B
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
nsv4387146	copy number variation	4	nstd173	human		GRCh37 chr6: 152,343,718-152,369,169 , GRCh38.p12 chr6: 152,022,583-152,048,034	ESR1
nsv4371674	copy number variation	102	nstd173	human		GRCh37 chr3: 89,394,610-89,419,375 , GRCh38.p12 chr3: 89,345,460-89,370,225	EPHA3
nsv4372603	copy number variation	1	nstd173	human		GRCh37 chr3: 21,254,370-21,351,637 , GRCh38.p12 chr3: 21,212,878-21,310,145	LOC105376988
nsv4369101	copy number variation	83	nstd173	human		GRCh37 chr11: 18,941,197-18,962,398 , GRCh38.p12 chr11: 18,919,650-18,940,851	MRGPRX1
nsv4371533	copy number variation	83	nstd173	human		GRCh37 chr1: 72,762,663-72,811,135 , GRCh38.p12 chr1: 72,296,980-72,345,452 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,677	RPL31P12, LOC105378797
nsv4365341	copy number variation	37	nstd173	human		GRCh37 chr14: 24,445,622-24,479,697 , GRCh38.p12 chr14: 23,976,413-24,010,488 , GRCh38.p12 chr14\|NW_018654722.1: 273,828-316,310	DHRS4L2, DHRS4L1
nsv4371731	copy number variation	44	nstd173	human		GRCh37 chr19: 41,352,689-41,385,370 , GRCh38.p12 chr19: 40,846,784-40,879,465	CYP2A7, CYP2A6
nsv4378163	copy number variation	14	nstd173	human		GRCh37 chr6: 254,254-280,386 , GRCh38.p12 chr6: 254,254-280,386	,
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
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 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
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4381624	copy number variation	39	nstd173	human		GRCh37 chr1: 155,180,848-155,211,654 , GRCh38.p12 chr1: 155,211,057-155,241,863	GBA1LP, MTX1, 2 more genes
nsv4368752	copy number variation	2	nstd173	human		GRCh37 chr6: 95,473,773-95,567,005 , GRCh38.p12 chr6: 94,764,055-94,857,287	0
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4388385	copy number variation	148	nstd173	human		GRCh37 chr14: 106,537,003-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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1-0514-002 AND nstd173 (20)
dbVar
PREDICTED: Homo sapiens LIM domain only 2 (LMO2), transcript variant X5, mRNA
PREDICTED: Homo sapiens LIM domain only 2 (LMO2), transcript variant X5, mRNA
gi|2462525193|ref|XM_054368774.1|

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