1-0936-003 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
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
nsv4372685	copy number variation	21	nstd173	human		GRCh37 chr5: 9,897,967-9,926,410 , GRCh38.p12 chr5: 9,897,855-9,926,298	LINC02112
nsv4373449	copy number variation	132	nstd173	human		GRCh37 chr2: 98,138,417-98,162,176 , GRCh38.p12 chr2: 97,521,954-97,545,713	ANKRD36B
nsv4366472	copy number variation	183	nstd173	human		GRCh37 chr3: 46,793,072-46,849,588 , GRCh38.p12 chr3: 46,751,582-46,808,098	PRSS44P, PRSS43P
nsv4372118	copy number variation	1	nstd173	human		GRCh37 chr11: 22,045,523-22,271,567 , GRCh38.p12 chr11: 22,023,977-22,250,021	LOC102723370, ANO5
nsv4369067	copy number variation	1	nstd173	human		GRCh37 chr11: 21,564,531-21,698,005 , GRCh38.p12 chr11: 21,542,985-21,676,459	NELL1,
nsv4381073	copy number variation	1	nstd173	human		GRCh37 chr12: 76,519,960-76,588,448 , GRCh38.p12 chr12: 76,126,180-76,194,668	LOC641695, RNU6-1271P
nsv4388544	copy number variation	68	nstd173	human		GRCh37 chrX: 62,470,734-62,505,606 , GRCh38.p12 chrX: 63,250,857-63,285,729	LOC105377212, LOC100533730
nsv4379967	copy number variation	33	nstd173	human		GRCh37 chr1: 49,914,804-49,997,674 , GRCh38.p12 chr1: 49,449,132-49,532,002	LOC107984954, AGBL4-IT1, 1 more genes
nsv4367877	copy number variation	1	nstd173	human		GRCh37 chrX: 1,459,626-1,506,403 , GRCh38.p12 chrX: 1,340,733-1,387,510	IL3RA, LOC101928032, 2 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
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 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
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 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
nsv4372679	copy number variation	125	nstd173	human		GRCh37 chr14: 74,001,111-74,029,899 , GRCh38.p12 chr14: 73,534,407-73,563,195	HEATR4, ACOT1, 1 more genes
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4367426	copy number variation	1	nstd173	human		GRCh37 chr20: 41,532,600-42,368,502 , GRCh38.p12 chr20: 42,903,960-43,739,862	LOC101927200, LOC107985380, 17 more genes

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1-0936-003 AND nstd173 (19)
dbVar
3-0380-002 AND nstd173 (29)
dbVar
OMIM Links for GEO Profiles (Select 121723236) (1)
OMIM
MAOB monoamine oxidase B [Homo sapiens]
MAOB monoamine oxidase B [Homo sapiens]
Gene ID:4129

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Gene Links for GEO Profiles (Select 1010752) (1)
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