MS16921 AND nstd71 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv888606	copy number variation	30	nstd71	human		NCBI36 chr7: 82,967,319-83,031,305 , GRCh37.p13 chr7: 83,129,383-83,193,369 , GRCh38.p12 chr7: 83,500,067-83,564,053	SEMA3E
nsv881222	copy number variation	185	nstd71	human		NCBI36 chr4: 162,058,162-162,152,452 , GRCh37.p13 chr4: 161,838,712-161,933,002 , GRCh38.p12 chr4: 160,917,560-161,011,850	LOC105377513
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
nsv883997	copy number variation	2	nstd71	human		NCBI36 chr6: 30,032,707-30,045,520 , GRCh37.p13 chr6\|NT_167246.1: 1,223,330-1,236,118 , GRCh37.p13 chr6\|NT_167247.1: 1,306,603-1,319,395 , GRCh37.p13 chr6: 29,924,728-29,937,541 , GRCh38.p12 chr6\|NT_167247.2: 1,301,018-1,313,810 , GRCh38.p12 chr6: 29,956,951-29,969,764 , GRCh38.p12 chr6\|NT_167246.2: 1,217,710-1,230,498	MICD, HLA-W
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
nsv892178	copy number variation	3	nstd71	human		NCBI36 chr9: 6,663,957-6,740,556 , GRCh37.p13 chr9: 6,673,957-6,750,556 , GRCh38.p12 chr9: 6,673,957-6,750,556	LINC02851, RPL35AP20, 3 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
nsv908125	copy number variation	4	nstd71	human		NCBI36 chr17: 31,462,326-31,567,477 , GRCh37.p13 chr17\|NW_003315949.1: 1-65,496 , GRCh37.p13 chr17: 34,438,213-34,543,364 , GRCh38.p12 chr17: 36,110,820-36,215,910 , GRCh38.p12 chr17\|NT_187661.1: 64,917-134,851 , GRCh38.p12 chr17\|NT_187614.1: 345,741-415,644	CCL4L2, LOC101927369, 7 more genes

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