SP52416 AND nstd71 - dbVar - NCBI

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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
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
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv885819	copy number variation	1	nstd71	human		NCBI36 chr6: 38,256,748-38,298,417 , GRCh37.p13 chr6: 38,148,770-38,190,439 , GRCh38.p12 chr6: 38,180,994-38,222,663	BTBD9
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
nsv908564	copy number variation	4	nstd71	human		NCBI36 chr17: 42,777,627-42,877,310 , GRCh37.p13 chr17: 45,422,628-45,522,311 , GRCh38.p12 chr17: 47,345,262-47,444,945	EFCAB13, NFE2L3P2, 1 more genes
nsv895252	copy number variation	2	nstd71	human		NCBI36 chr10: 47,007,374-47,171,576 , GRCh37.p13 chr10\|NW_003871068.1: 437,247-589,544 , GRCh37.p13 chr10: 47,537,368-47,689,665 , GRCh38.p12 chr10: 46,166,132-46,330,334	LOC105378577, ANTXRLP1, 2 more genes
nsv902531	copy number variation	3	nstd71	human		NCBI36 chr14: 105,108,671-105,217,427 , GRCh37.p13 chr14: 106,037,626-106,146,382 , GRCh37.p13 chr14\|NW_004166863.1: 234,456-343,212 , GRCh38.p12 chr14: 105,571,289-105,680,045 , GRCh38.p12 chr14\|NT_187600.1: 38,287-147,814	IGHGP, , 11 more genes
nsv906417	copy number variation	125	nstd71	human		NCBI36 chr16: 32,469,358-32,511,911 , GRCh37.p13 chr16: 32,561,857-32,604,410 , GRCh38.p12 chr16: 32,550,536-32,593,089	0
nsv906159	copy number variation	6	nstd71	human		NCBI36 chr16: 32,438,272-32,449,148 , GRCh37.p13 chr16: 32,530,771-32,541,647 , GRCh38.p12 chr16: 32,519,450-32,530,326	0
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
nsv901150	copy number variation	5	nstd71	human		NCBI36 chr14: 19,093,120-19,226,775 , GRCh37.p13 chr14: 20,023,120-20,156,935 , GRCh38.p12 chr14: 19,611,715-19,688,776	LOC100420171, USP10P1, 5 more genes
nsv889073	copy number variation	3	nstd71	human		NCBI36 chr7: 116,340,095-116,398,349 , GRCh37.p13 chr7: 116,552,859-116,611,113 , GRCh38.p12 chr7: 116,912,805-116,971,059	CAPZA2, ST7, 5 more genes
nsv903278	copy number variation	8	nstd71	human		NCBI36 chr15: 19,768,826-20,203,694 , GRCh37.p13 chr15: 22,267,462-22,652,330 , GRCh38.p12 chr15: 21,979,511-22,308,242	IGHV1OR15-4, OR4N3P, 18 more genes

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