SP81333 AND nstd71 - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv908357	copy number variation	27	nstd71	human		NCBI36 chr17: 41,771,015-41,922,658 , GRCh37.p13 chr17: 44,415,257-44,566,775 , GRCh38.p12 chr17: 46,337,891-46,489,976	, LRRC37A, 2 more genes
nsv873049	copy number variation	42	nstd71	human		NCBI36 chr1: 195,077,621-195,199,868 , GRCh37.p13 chr1: 196,810,998-196,933,245 , GRCh38.p12 chr1: 196,841,868-196,964,115	CFHR2, CFHR4, 2 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv879427	copy number variation	1	nstd71	human		NCBI36 chr4: 70,216,715-70,309,146 , GRCh37.p13 chr4: 70,182,126-70,274,557 , GRCh38.p12 chr4: 69,316,408-69,408,839	UGT2B25P, LOC642496, 3 more genes
nsv891146	copy number variation	1	nstd71	human		NCBI36 chr8: 86,910,517-87,152,863 , GRCh37.p13 chr8: 86,841,229-87,083,747 , GRCh38.p12 chr8: 85,829,000-86,071,518	LOC107986954, LINC02849, 3 more genes
nsv879383	copy number variation	6	nstd71	human		NCBI36 chr4: 70,030,098-70,081,519 , GRCh37.p13 chr4: 69,995,509-70,046,930 , GRCh38.p12 chr4: 69,129,791-69,181,212	LOC101060162, LOC105377267, 1 more genes
nsv911352	copy number variation	32	nstd71	human		NCBI36 chr19: 20,386,247-20,522,325 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-464,932 , GRCh37.p13 chr19: 20,522,409-20,730,485 , GRCh38.p12 chr19: 20,411,600-20,547,679	LOC105372316, LOC105372317, 4 more genes
nsv902763	copy number variation	14	nstd71	human		NCBI36 chr15: 19,031,743-19,248,452 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,566,406-21,352,165	RNU6-749P, LOC283804, 33 more genes
nsv914607	copy number variation	103	nstd71	human		NCBI36 chr22: 22,600,777-22,713,954 , GRCh37.p13 chr22: 24,270,777-24,383,954 , GRCh38.p12 chr22\|NT_187633.1: 192,395-278,129	LOC100420769, DDT, 10 more genes
nsv887653	copy number variation	3	nstd71	human		NCBI36 chr7: 13,235,440-13,273,491 , GRCh37.p13 chr7: 13,268,915-13,306,966 , GRCh38.p12 chr7: 13,229,290-13,267,341	0
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv905826	copy number variation	2	nstd71	human		NCBI36 chr16: 32,258,794-32,579,320 , GRCh37.p13 chr16: 32,351,293-32,671,819 , GRCh38.p12 chr16: 32,339,972-32,660,498	ABCD1P3, ACTR3BP3, 5 more genes
nsv903078	copy number variation	34	nstd71	human		NCBI36 chr15: 19,341,464-19,556,128 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,924,655-21,498,353	OR11J2P, LOC105370715, 23 more genes

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SP81333 AND nstd71 (14)
dbVar
OMIM Links for Nucleotide (Select 1890333606) (3)
OMIM
OMIM Links for Nucleotide (Select 1890272231) (3)
OMIM
Related DataSets for GEO Profiles (Select 27127265) (1)
GEO DataSets
Transcription factor IIF cofactor GAS41 overexpression
Transcription factor IIF cofactor GAS41 overexpression
Accession: GDS2170

GEO DataSets

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