12-4425-001 AND nstd173 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4369234	copy number variation	1	nstd173	human		GRCh37 chr2: 51,778,758-51,827,522 , GRCh38.p12 chr2: 51,551,620-51,600,384	NRXN1-DT
nsv4384041	copy number variation	19	nstd173	human		GRCh37 chr19: 53,525,534-53,552,228 , GRCh38.p12 chr19: 53,022,281-53,048,975	ERVV-2
nsv4367952	copy number variation	7	nstd173	human		GRCh37 chr18: 4,459,854-4,494,127 , GRCh38.p12 chr18: 4,459,854-4,494,127	LOC105371968, ELOCP27
nsv4375790	copy number variation	2	nstd173	human		GRCh37 chr8: 39,230,312-39,389,016 , GRCh38.p12 chr8: 39,372,793-39,531,497	ADAM5, ADAM3A
nsv4380312	copy number variation	2	nstd173	human		GRCh37 chr16: 7,032,320-7,138,711 , GRCh38.p12 chr16: 6,982,319-7,088,710	RBFOX1, LOC105371068, 1 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
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
nsv4366309	copy number variation	2	nstd173	human		GRCh37 chr6: 254,254-294,463 , GRCh38.p12 chr6: 254,254-294,463	, DUSP22, 1 more genes
nsv4383713	copy number variation	36	nstd173	human		GRCh37 chr12: 11,220,827-11,251,705 , GRCh38.p12 chr12: 11,068,228-11,099,106	TAS2R64P, TAS2R43, 3 more genes
nsv4383534	copy number variation	1	nstd173	human		GRCh37 chrX: 138,808,851-139,342,599 , GRCh38.p12 chrX: 139,726,692-140,260,434	CXorf66, LOC728660, 7 more genes
nsv4380168	copy number variation	295	nstd173	human		GRCh37 chr17: 44,187,492-44,784,639 , GRCh38.p12 chr17: 46,110,126-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 812,225-1,226,699	MAPK8IP1P1, DND1P2, 14 more genes
nsv4385857	copy number variation	1	nstd173	human		GRCh37 chr14: 22,689,654-22,960,757 , GRCh38.p12 chr14: 22,221,755-22,491,770	TRDV2, TRDJ3, 38 more genes
nsv4385529	copy number variation	179	nstd173	human		GRCh37 chr14: 106,525,299-106,692,891 , GRCh38.p12 chr14: 106,069,054-106,236,281 , GRCh38.p12 chr14\|NT_187600.1: 536,823-704,050	IGHVIII-13-1, IGHV1-18, 19 more genes

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12-4425-001 AND nstd173 (16)
dbVar
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Accession: GDS3613

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PMC Links for GEO Profiles (Select 6194064) (97)
PMC

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