SP52393 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
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
nsv890635	copy number variation	3	nstd71	human		NCBI36 chr8: 20,025,584-20,048,921 , GRCh37.p13 chr8: 19,981,304-20,004,641 , GRCh38.p12 chr8: 20,123,793-20,147,130	LOC105379312, SLC18A1
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
nsv884564	copy number variation	2	nstd71	human		NCBI36 chr6: 32,058,245-32,069,461 , GRCh37.p13 chr6\|NT_167245.1: 3,235,847-3,247,064 , GRCh37.p13 chr6\|NT_167249.1: 3,282,976-3,294,192 , GRCh37.p13 chr6: 31,950,266-31,961,482 , GRCh38.p12 chr6: 31,982,489-31,993,705 , GRCh38.p12 chr6\|NT_167245.2: 3,230,262-3,241,479 , GRCh38.p12 chr6\|NT_167249.2: 3,283,678-3,294,894	C4B_2, C4A
nsv879309	copy number variation	1	nstd71	human		NCBI36 chr4: 69,076,346-69,163,188 , GRCh37.p13 chr4: 69,393,751-69,480,593 , GRCh38.p12 chr4: 68,528,033-68,614,875	UGT2B17, LOC100132651, 1 more genes
nsv894840	copy number variation	5	nstd71	human		NCBI36 chr10: 6,702,141-6,885,243 , GRCh37.p13 chr10: 6,662,135-6,845,237 , GRCh38.p12 chr10: 6,620,173-6,803,275	LINP1, LINC02648, 2 more genes
nsv871734	copy number variation	29	nstd71	human		NCBI36 chr1: 12,771,679-12,845,198 , GRCh37.p13 chr1: 12,849,092-12,922,611 , GRCh38.p12 chr1: 12,788,951-12,862,756 , GRCh38.p12 chr1\|NW_012132914.1: 1-44,269	HNRNPCL1, LINC01784, 4 more genes

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