1-0748-003 AND nstd173 - dbVar - NCBI

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Items: 18

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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
nsv4388369	copy number variation	2	nstd173	human		GRCh37 chr7: 141,755,372-141,799,159 , GRCh38.p12 chr7: 142,055,572-142,099,359 , GRCh38.p12 chr7\|NT_187562.1: 17,452-61,239	MGAM
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4370292	copy number variation	2	nstd173	human		GRCh37 chr5: 3,953,891-3,978,902 , GRCh38.p12 chr5: 3,953,777-3,978,788	LOC105374626
nsv4376740	copy number variation	1	nstd173	human		GRCh37 chr5: 177,856,422-177,877,713 , GRCh38.p12 chr5: 178,429,421-178,450,712	COL23A1
nsv4372565	copy number variation	18	nstd173	human		GRCh37 chr13: 57,758,288-57,778,379 , GRCh38.p12 chr13: 57,184,154-57,204,245	MTCO2P3
nsv4375689	copy number variation	34	nstd173	human		GRCh37 chr20: 1,557,189-1,597,997 , GRCh38.p12 chr20: 1,576,543-1,617,351	SIRPB1
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
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
nsv4377200	copy number variation	2	nstd173	human		GRCh37 chr10: 45,215,162-45,367,803 , GRCh38.p12 chr10: 44,719,714-44,872,355	EIF2AP4, TMEM72-AS1
nsv4380606	copy number variation	21	nstd173	human		GRCh37 chr7: 43,361-79,263 , GRCh38.p12 chr7: 43,361-79,263 , GRCh38.p12 chr7\|NT_187558.1: 1-35,362 , GRCh38.p12 chr7\|NT_187653.1: 35,682-71,584	LOC101929756, LOC105375113
nsv4366631	copy number variation	46	nstd173	human		GRCh37 chr12: 11,220,827-11,256,413 , GRCh38.p12 chr12: 11,068,228-11,103,814	PRH1, TAS2R64P, 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
nsv4382393	copy number variation	1	nstd173	human		GRCh37 chrX: 1,223,288-1,358,846 , GRCh38.p12 chrX: 1,123,135-1,239,953	CRLF2, LOC100418703, 2 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
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4371199	copy number variation	115	nstd173	human		GRCh37 chr2: 52,738,983-52,790,493 , GRCh38.p12 chr2: 52,511,845-52,563,355	0
nsv4377013	copy number variation	26	nstd173	human		GRCh37 chr5: 180,378,754-180,442,388 , GRCh38.p12 chr5: 180,951,754-181,015,388	BTNL3, TMEM69P2, 4 more genes

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