SP50522 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
nsv878754	copy number variation	1	nstd71	human		NCBI36 chr4: 22,628,668-22,755,985 , GRCh37.p13 chr4: 23,019,570-23,146,887 , GRCh38.p12 chr4: 23,017,947-23,145,264	LOC105374524
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv885195	copy number variation	2	nstd71	human		NCBI36 chr6: 32,615,216-32,633,666 , GRCh37.p13 chr6: 32,507,238-32,525,688 , GRCh38.p12 chr6: 32,539,461-32,557,911	HLA-DRB6, RNU1-61P
nsv905952	copy number variation	17	nstd71	human		NCBI36 chr16: 32,406,646-32,579,320 , GRCh37.p13 chr16: 32,499,145-32,671,819 , GRCh38.p12 chr16: 32,487,824-32,660,498	LOC107984013, FAM153DP
nsv895573	copy number variation	1	nstd71	human		NCBI36 chr10: 65,276,235-65,368,946 , GRCh37.p13 chr10: 65,606,229-65,698,940 , GRCh38.p12 chr10: 63,846,469-63,939,180	LOC101928859, RPL7AP50
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
nsv914684	copy number variation	27	nstd71	human		NCBI36 chr22: 23,991,725-24,113,704 , GRCh37.p13 chr22: 25,661,725-25,783,704 , GRCh38.p12 chr22: 25,265,758-25,387,737	LRP5L, IGLL3P, 2 more genes
nsv873875	copy number variation	3	nstd71	human		NCBI36 chr2: 36,234,999-36,285,895 , GRCh37.p13 chr2: 36,381,495-36,432,391 , GRCh38.p12 chr2: 36,154,352-36,205,248	0
nsv884256	copy number variation	61	nstd71	human		NCBI36 chr6: 31,388,306-31,396,472 , GRCh37.p13 chr6: 31,280,327-31,288,493 , GRCh37.p13 chr6\|NT_167246.1: 2,627,146-2,631,393 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,622,207 , GRCh38.p12 chr6\|NT_167246.2: 2,621,526-2,625,775 , GRCh38.p12 chr6: 31,312,550-31,320,716 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,622,909	0
nsv880191	copy number variation	6	nstd71	human		NCBI36 chr4: 145,012,409-145,259,965 , GRCh37.p13 chr4: 144,792,959-145,040,515 , GRCh38.p12 chr4: 143,871,806-144,119,362	GYPA, GYPE, 6 more genes
nsv874523	copy number variation	4	nstd71	human		NCBI36 chr2: 87,226,520-87,375,788 , GRCh37.p13 chr2: 87,373,009-87,522,277 , GRCh38.p12 chr2: 87,145,886-87,295,154	CENPNP1, LOC102724642, 4 more genes
nsv914929	copy number variation	13	nstd71	human		NCBI36 chr22: 24,215,704-24,244,593 , GRCh37.p13 chr22: 25,885,704-25,914,593 , GRCh38.p12 chr22: 25,489,737-25,518,626	0

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SP50522 AND nstd71 (14)
dbVar
ELMOD2 ELMO domain containing 2 [Homo sapiens]
ELMOD2 ELMO domain containing 2 [Homo sapiens]
Gene ID:255520

Gene
Gene Links for Nucleotide (Select 1519243963) (1)
Gene
SRA Links for BioSample (Select 2776310) (1)
SRA
OMIM Links for Gene (Select 5106) (2)
OMIM

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