SP51235 AND nstd71 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
nsv908398	copy number variation	38	nstd71	human		NCBI36 chr17: 41,780,482-41,922,658 , GRCh37.p13 chr17: 44,424,726-44,566,775 , GRCh38.p12 chr17: 46,347,360-46,489,976	NSFP1, ARL17B
nsv888231	copy number variation	61	nstd71	human		NCBI36 chr7: 62,366,659-62,440,767 , GRCh37.p13 chr7: 62,729,224-62,803,332 , GRCh38.p12 chr7: 63,268,846-63,342,954	ZNF733P, ARAFP3
nsv885377	copy number variation	3	nstd71	human		NCBI36 chr6: 32,636,891-32,668,837 , GRCh37.p13 chr6: 32,528,913-32,560,859 , GRCh38.p12 chr6: 32,561,136-32,593,082	RNU1-152P, HLA-DRB1
nsv891536	copy number variation	1	nstd71	human		NCBI36 chr8: 141,726,315-141,916,431 , GRCh37.p13 chr8: 141,657,133-141,847,249 , GRCh38.p12 chr8: 140,647,034-140,837,150	PTK2, MIR151A
nsv893265	copy number variation	25	nstd71	human		NCBI36 chr9: 43,609,749-43,730,292 , GRCh37.p13 chr9: 43,669,753-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,144,636	CNTNAP3B, LOC100420440
nsv911843	copy number variation	5	nstd71	human		NCBI36 chr19: 47,997,996-48,107,283 , GRCh37.p13 chr19: 43,306,156-43,415,443 , GRCh38.p12 chr19: 42,802,004-42,911,291	PSG10P, PSG1, 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
nsv907853	copy number variation	28	nstd71	human		NCBI36 chr17: 18,971,335-19,040,640 , GRCh37.p13 chr17: 19,030,610-19,100,047 , GRCh38.p12 chr17: 19,127,297-19,196,734	SNORD3C, GRAPL-AS1, 3 more genes
nsv886198	copy number variation	304	nstd71	human		NCBI36 chr6: 77,073,066-77,088,077 , GRCh37.p13 chr6: 77,016,346-77,031,357 , GRCh38.p12 chr6: 76,306,629-76,321,640	0
nsv896955	copy number variation	127	nstd71	human		NCBI36 chr11: 5,828,407-5,911,385 , GRCh37.p13 chr11: 5,871,831-5,954,809 , GRCh38.p12 chr11: 5,850,601-5,933,579	OR52E7P, OR52E4, 4 more genes
nsv902786	copy number variation	45	nstd71	human		NCBI36 chr15: 19,031,743-19,556,128 , GRCh37.p13 chr15: 20,771,729-22,141,158 , GRCh38.p12 chr15: 20,566,406-21,498,353	OR11J2P, RNU6-498P, 39 more genes
nsv895064	copy number variation	1	nstd71	human		NCBI36 chr10: 42,103,487-42,563,331 , GRCh37.p13 chr10: 42,783,481-43,243,325 , GRCh38.p12 chr10: 42,288,033-42,747,877	LINC02632, EIF3LP2, 13 more genes
nsv901372	copy number variation	21	nstd71	human		NCBI36 chr14: 19,301,051-19,486,339 , GRCh37.p13 chr14: 20,231,211-20,416,499 , GRCh38.p12 chr14: 19,763,052-19,948,340	LOC100421751, OR4N1P, 8 more genes

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SP51235 AND nstd71 (15)
dbVar
Related DataSets for GEO Profiles (Select 95010861) (1)
GEO DataSets
Myelodysplastic syndrome: CD34+ hematopoietic stem cells
Myelodysplastic syndrome: CD34+ hematopoietic stem cells
Accession: GDS3795

GEO DataSets
CSMD2-AS1 CSMD2 antisense RNA 1 [Homo sapiens]
CSMD2-AS1 CSMD2 antisense RNA 1 [Homo sapiens]
Gene ID:402779

Gene

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