MS20288 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
nsv872693	copy number variation	223	nstd71	human		NCBI36 chr1: 187,587,641-187,815,034 , GRCh37.p13 chr1: 189,321,018-189,548,411 , GRCh38.p12 chr1: 189,351,888-189,579,281	LOC105371657
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
nsv886441	copy number variation	2	nstd71	human		NCBI36 chr6: 100,189,704-100,536,638 , GRCh37.p13 chr6: 100,082,983-100,429,917 , GRCh38.p12 chr6: 99,635,107-99,982,041	MCHR2
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
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
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
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
nsv908554	copy number variation	80	nstd71	human		NCBI36 chr17: 42,005,250-42,092,850 , GRCh37.p13 chr17: 44,649,934-44,737,534 , GRCh38.p12 chr17: 46,572,568-46,660,168	ARL17A, LRRC37A2, 1 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
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
nsv886436	copy number variation	1	nstd71	human		NCBI36 chr6: 99,827,724-100,122,836 , GRCh37.p13 chr6: 99,721,003-100,016,115 , GRCh38.p12 chr6: 99,273,127-99,568,239	CCNC, COQ3, 5 more genes
nsv903294	copy number variation	22	nstd71	human		NCBI36 chr15: 19,777,876-19,993,878 , GRCh37.p13 chr15: 22,276,512-22,492,514 , GRCh38.p12 chr15: 21,988,561-22,204,563	OR4M2, OR4N4, 13 more genes
nsv901912	copy number variation	19	nstd71	human		NCBI36 chr14: 47,529,415-47,549,498 , GRCh37.p13 chr14: 48,459,665-48,479,748 , GRCh38.p12 chr14: 47,990,462-48,010,545	0

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