MS25755 AND nstd71 - dbVar - NCBI

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Items: 11

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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
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
nsv889766	copy number variation	46	nstd71	human		NCBI36 chr8: 2,110,516-2,133,500 , GRCh37.p13 chr8: 2,123,109-2,146,093 , GRCh37.p13 chr8\|NW_003571042.1: 157,720-180,704 , GRCh38.p12 chr8\|NT_187576.1: 358,319-381,303 , GRCh38.p12 chr8: 2,174,918-2,198,540	LOC105377782, LOC105377781
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv908379	copy number variation	346	nstd71	human		NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976	ARL17B, NSFP1, 1 more genes
nsv895735	copy number variation	1	nstd71	human		NCBI36 chr10: 79,168,987-79,286,611 , GRCh37.p13 chr10: 79,498,981-79,616,605 , GRCh38.p12 chr10\|NT_187580.1: 1-95,539 , GRCh38.p12 chr10: 77,739,223-77,856,847	DLG5, IMPDH1P5, 2 more genes
nsv904023	copy number variation	257	nstd71	human		NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691	LOC100422491, GOLGA8B, 5 more genes
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
nsv895755	copy number variation	3	nstd71	human		NCBI36 chr10: 81,392,532-81,497,813 , GRCh37.p13 chr10: 81,402,490-81,507,631 , GRCh38.p12 chr10: 79,642,734-79,747,875	BEND3P3, NUTM2B, 4 more genes
nsv878628	copy number variation	13	nstd71	human		NCBI36 chr4: 8,780,538-9,095,677 , GRCh37.p13 chr4: 8,729,638-9,486,579 , GRCh38.p12 chr4: 8,727,912-9,484,932	FAM86KP, DEFB108F, 42 more genes
nsv906269	copy number variation	1	nstd71	human		NCBI36 chr16: 32,443,949-32,475,100 , GRCh37.p13 chr16: 32,536,448-32,567,599 , GRCh38.p12 chr16: 32,525,127-32,556,278	0

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