SP81127 AND nstd71 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv900450	copy number variation	3	nstd71	human		NCBI36 chr13: 68,147,928-68,259,506 , GRCh37.p13 chr13: 69,249,927-69,361,505 , GRCh38.p12 chr13: 68,675,795-68,787,373	RN7SL761P
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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv895761	copy number variation	319	nstd71	human		NCBI36 chr10: 81,462,715-81,497,813 , GRCh37.p13 chr10: 81,472,521-81,507,631 , GRCh38.p12 chr10: 79,712,765-79,747,875	NUTM2B, NUTM2B-AS1
nsv908380	copy number variation	142	nstd71	human		NCBI36 chr17: 41,775,690-41,943,845 , GRCh37.p13 chr17: 44,419,932-44,588,529 , GRCh38.p12 chr17: 46,342,566-46,511,163	LRRC37A2, ARL17A, 3 more genes
nsv900152	copy number variation	33	nstd71	human		NCBI36 chr13: 56,638,784-56,698,642 , GRCh37.p13 chr13: 57,740,783-57,800,641 , GRCh38.p12 chr13: 57,166,649-57,226,507	MTCO2P3, LOC105370216, 2 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv890102	copy number variation	13	nstd71	human		NCBI36 chr8: 7,184,351-7,342,249 , GRCh37.p13 chr8: 7,196,941-7,354,839 , GRCh38.p12 chr8\|NT_187570.1: 78,282-180,420 , GRCh38.p12 chr8: 7,339,419-7,497,317	DEFB106B, DEFB104B, 10 more genes
nsv906222	copy number variation	2	nstd71	human		NCBI36 chr16: 32,439,428-32,505,195 , GRCh37.p13 chr16: 32,531,927-32,597,694 , GRCh38.p12 chr16: 32,520,606-32,586,373	0
nsv873691	copy number variation	49	nstd71	human		NCBI36 chr2: 18,027,050-18,062,826 , GRCh37.p13 chr2: 18,163,569-18,199,345 , GRCh38.p12 chr2: 17,982,303-18,018,079	0

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SP81127 AND nstd71 (12)
dbVar
PREDICTED: Homo sapiens LIM zinc finger domain containing 2 (LIMS2), transcript ...
PREDICTED: Homo sapiens LIM zinc finger domain containing 2 (LIMS2), transcript variant X11, mRNA
gi|2217329408|ref|XM_047444975.1|

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