157178 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
nsv4380190	copy number variation	32	nstd173	human		GRCh37 chr2: 98,079,569-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713	ANKRD36B
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
nsv4380251	copy number variation	13	nstd173	human		GRCh37 chr19: 41,345,327-41,392,653 , GRCh38.p12 chr19: 40,839,422-40,886,748	CYP2A7, CYP2A6
nsv4373933	copy number variation	2	nstd173	human		GRCh37 chr10: 5,061,766-5,121,206 , GRCh38.p12 chr10: 5,019,574-5,079,014	LOC107984198, AKR1C3
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
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4385330	copy number variation	98	nstd173	human		GRCh37 chr6: 257,340-294,826 , GRCh38.p12 chr6: 257,340-294,826	, , 1 more genes
nsv4377906	copy number variation	34	nstd173	human		GRCh37 chr5: 180,378,754-180,416,782 , GRCh38.p12 chr5: 180,951,754-180,989,782	BTNL8, ARPP19P1, 3 more genes
nsv4370846	copy number variation	105	nstd173	human		GRCh37 chr12: 11,216,817-11,251,861 , GRCh38.p12 chr12: 11,064,218-11,099,262	PRH1, PRH1-PRR4, 3 more genes
nsv4373711	copy number variation	238	nstd173	human		GRCh37 chr14: 74,001,111-74,031,034 , GRCh38.p12 chr14: 73,534,407-73,564,330	NT5CP2, HEATR4, 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
nsv4378688	copy number variation	2	nstd173	human		GRCh37 chr3: 155,064,769-155,092,531 , GRCh38.p12 chr3: 155,346,980-155,374,742	0
nsv4378481	copy number variation	186	nstd173	human		GRCh37 chr2: 4,208,245-4,234,699 , GRCh38.p12 chr2: 4,160,655-4,187,109	0
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
nsv4386728	copy number variation	1	nstd173	human		GRCh37 chr16: 82,172,142-83,676,947 , GRCh38.p12 chr16: 82,138,537-83,643,342	LOC101928446, MIR8058, 9 more genes
nsv4381892	copy number variation	1	nstd173	human		GRCh37 chr14: 22,461,404-22,975,728 , GRCh38.p12 chr14: 21,993,164-22,506,743	TRAV27, TRAV41, 73 more genes
nsv4372404	copy number variation	32	nstd173	human		GRCh37 chr7: 142,338,344-142,493,638 , GRCh38.p12 chr7: 142,630,828-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, PRSS3P2, 21 more genes
nsv4374050	copy number variation	11	nstd173	human		GRCh37 chr3: 162,528,531-162,626,676 , GRCh38.p12 chr3: 162,810,743-162,908,888	0
nsv4380787	copy number variation	76	nstd173	human		GRCh37 chr7: 38,294,983-38,387,020 , GRCh38.p12 chr7: 38,255,382-38,347,419	TRG, TRGV5P, 18 more genes

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157178 AND nstd173 (20)
dbVar
222679 AND nstd173 (13)
dbVar
Related DataSets for GEO Profiles (Select 838517) (1)
GEO DataSets
HIV viral infection time course
HIV viral infection time course
Accession: GDS171

GEO DataSets
Homo sapiens C-type lectin domain family 4, member C, mRNA (cDNA clone MGC:12579...
Homo sapiens C-type lectin domain family 4, member C, mRNA (cDNA clone MGC:125791 IMAGE:40030336), complete cds
gi|74354484|gb|BC102015.1|

Nucleotide

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