1-0286-002 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv4374961	copy number variation	9	nstd173	human		GRCh37 chr11: 18,941,197-18,961,725 , GRCh38.p12 chr11: 18,919,650-18,940,178	MRGPRX1
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
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
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
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
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4379968	copy number variation	1	nstd173	human		GRCh37 chr6: 254,283-294,836 , GRCh38.p12 chr6: 254,283-294,836	, , 1 more genes
nsv4367001	copy number variation	197	nstd173	human		GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4373659	copy number variation	1	nstd173	human		GRCh37 chr6: 19,210,417-19,245,127 , GRCh38.p12 chr6: 19,210,186-19,244,896	0
nsv4381200	copy number variation	5	nstd173	human		GRCh37 chr4: 64,693,916-64,723,180 , GRCh38.p12 chr4: 63,828,198-63,857,462	0
nsv4387490	copy number variation	1	nstd173	human		GRCh37 chrX: 1,734,398-2,001,459 , GRCh38.p12 chrX: 1,615,505-1,882,566	ASMT, LOC105379413, 5 more genes
nsv4372736	copy number variation	43	nstd173	human		GRCh37 chr10: 46,966,534-47,149,411 , GRCh38.p12 chr10: 46,400,352-46,583,083	NPY4R, SYT15-AS1, 5 more genes
nsv4386048	copy number variation	1	nstd173	human		GRCh37 chr14: 22,599,356-22,959,362 , GRCh38.p12 chr14: 22,131,394-22,490,374	TRDD2, TRDV3, 46 more genes
nsv4366571	copy number variation	33	nstd173	human		GRCh37 chr16: 34,466,679-34,755,828 , GRCh38.p12 chr16: 35,232,308-35,521,457	FGFR3P5, FRG2HP, 26 more genes
nsv4370677	copy number variation	26	nstd173	human		GRCh37 chr7: 38,294,983-38,356,732 , GRCh38.p12 chr7: 38,255,382-38,317,131	TRGV11, TRG, 11 more genes

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1-0286-002 AND nstd173 (19)
dbVar
Homologene neighbors for GEO Profiles (Select 115471056) (0)
GEO Profiles
FARS2 phenylalanyl-tRNA synthetase 2, mitochondrial [Homo sapiens]
FARS2 phenylalanyl-tRNA synthetase 2, mitochondrial [Homo sapiens]
Gene ID:10667

Gene
Gene Links for OMIM (Select 617046) (1)
Gene

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