SP51134 AND nstd71 - dbVar - NCBI

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Items: 13

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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
nsv901814	copy number variation	288	nstd71	human		NCBI36 chr14: 43,558,217-43,606,201 , GRCh37.p13 chr14: 44,488,467-44,536,451 , GRCh38.p12 chr14: 44,019,264-44,067,248	LINC02307
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
nsv885177	copy number variation	1	nstd71	human		NCBI36 chr6: 32,613,708-32,625,376 , GRCh37.p13 chr6: 32,505,730-32,517,398 , GRCh38.p12 chr6\|NT_167246.2: 3,827,282-3,833,179 , GRCh38.p12 chr6: 32,537,953-32,549,621	RNU1-61P
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
nsv911984	copy number variation	10	nstd71	human		NCBI36 chr19: 48,146,458-48,213,514 , GRCh37.p13 chr19: 43,454,618-43,521,674 , GRCh38.p12 chr19: 42,950,466-43,017,522	PSG11, CEACAMP7
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
nsv912042	copy number variation	22	nstd71	human		NCBI36 chr19: 48,235,556-48,418,735 , GRCh37.p13 chr19: 43,543,716-43,726,895 , GRCh38.p12 chr19: 43,039,564-43,222,743	PSG2, LOC284344, 7 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv904039	copy number variation	243	nstd71	human		NCBI36 chr15: 32,506,097-32,625,184 , GRCh37.p13 chr15: 34,718,805-34,837,892 , GRCh38.p12 chr15: 34,426,604-34,545,691	DNM1P5, MIR1233-2, 4 more genes
nsv913750	copy number variation	5	nstd71	human		NCBI36 chr21: 41,208,473-41,241,269 , GRCh37.p13 chr21: 42,286,603-42,319,399 , GRCh38.p12 chr21: 40,914,677-40,947,473	0
nsv903228	copy number variation	62	nstd71	human		NCBI36 chr15: 19,635,853-19,993,878 , GRCh37.p13 chr15: 21,371,194-22,492,514 , GRCh38.p12 chr15: 21,165,865-22,204,563	LOC642131, IGHV1OR15-4, 52 more genes
nsv890102	copy number variation	13	nstd71	human		NCBI36 chr8: 7,184,351-7,342,249 , GRCh37.p13 chr8: 7,196,941-7,354,839 , GRCh38.p12 chr8\|NT_187570.1: 78,282-180,420 , GRCh38.p12 chr8: 7,339,419-7,497,317	DEFB106B, DEFB104B, 10 more genes

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