SP56396 AND nstd71 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv886268	copy number variation	64	nstd71	human		NCBI36 chr6: 79,031,809-79,098,352 , GRCh37.p13 chr6: 78,975,090-79,041,633 , GRCh38.p12 chr6: 78,265,373-78,331,916	LOC105377865
nsv903945	copy number variation	89	nstd71	human		NCBI36 chr15: 30,286,443-30,316,380 , GRCh37.p13 chr15: 32,499,151-32,529,088 , GRCh38.p12 chr15: 32,206,950-32,236,887	LOC102724078
nsv872973	copy number variation	15	nstd71	human		NCBI36 chr1: 194,923,360-194,928,236 , GRCh37.p13 chr1: 196,656,737-196,661,613 , GRCh38.p12 chr1: 196,687,607-196,692,483	CFH
nsv892282	copy number variation	1	nstd71	human		NCBI36 chr9: 9,780,403-9,788,092 , GRCh37.p13 chr9: 9,790,403-9,798,092 , GRCh38.p12 chr9: 9,790,403-9,798,092	LOC105375972, PTPRD
nsv895029	copy number variation	1	nstd71	human		NCBI36 chr10: 37,463,203-37,537,704 , GRCh37.p13 chr10: 37,423,197-37,497,698 , GRCh38.p12 chr10: 37,134,269-37,208,770	RNU6-811P, ANKRD30A
nsv883947	copy number variation	2	nstd71	human		NCBI36 chr6: 30,014,670-30,020,472 , GRCh37.p13 chr6: 29,906,691-29,912,493 , GRCh38.p12 chr6: 29,938,914-29,944,716	HLA-A, HCG4P5
nsv879344	copy number variation	30	nstd71	human		NCBI36 chr4: 69,117,497-69,173,198 , GRCh37.p13 chr4: 69,434,902-69,490,603 , GRCh38.p12 chr4: 68,569,184-68,624,885	UGT2B17, LOC100422402, 1 more genes
nsv898769	copy number variation	1	nstd71	human		NCBI36 chr12: 10,456,720-10,491,635 , GRCh37.p13 chr12: 10,565,453-10,600,368 , GRCh38.p12 chr12: 10,412,854-10,447,769	KLRC1, KLRC3, 1 more genes
nsv889356	copy number variation	1	nstd71	human		NCBI36 chr7: 143,506,472-143,704,886 , GRCh37.p13 chr7: 143,875,539-144,073,953 , GRCh38.p12 chr7: 144,178,446-144,376,860	ARHGEF34P, CTAGE4, 11 more genes
nsv907821	copy number variation	5	nstd71	human		NCBI36 chr17: 18,868,271-19,040,640 , GRCh37.p13 chr17: 18,927,546-19,100,047 , GRCh38.p12 chr17: 19,024,233-19,196,734	KYNUP1, SNORD3A, 10 more genes
nsv873946	copy number variation	60	nstd71	human		NCBI36 chr2: 41,084,366-41,109,046 , GRCh37.p13 chr2: 41,230,862-41,255,542 , GRCh38.p12 chr2: 41,003,722-41,028,402	0
nsv894935	copy number variation	32	nstd71	human		NCBI36 chr10: 20,882,037-20,902,433 , GRCh37.p13 chr10: 20,842,031-20,862,427 , GRCh38.p12 chr10: 20,553,102-20,573,498	0
nsv884849	copy number variation	16	nstd71	human		NCBI36 chr6: 32,561,832-32,576,147 , GRCh37.p13 chr6: 32,453,854-32,468,169 , GRCh38.p12 chr6: 32,486,077-32,500,392	0
nsv878767	copy number variation	1	nstd71	human		NCBI36 chr4: 26,060,424-26,072,588 , GRCh37.p13 chr4: 26,451,326-26,463,490 , GRCh38.p12 chr4: 26,449,704-26,461,868	0
nsv884227	copy number variation	223	nstd71	human		NCBI36 chr6: 31,385,967-31,397,263 , GRCh37.p13 chr6: 31,277,988-31,289,284 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,623,006 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh38.p12 chr6: 31,310,211-31,321,507 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,623,708 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775	0
nsv881456	copy number variation	7	nstd71	human		NCBI36 chr5: 738,748-869,095 , GRCh37.p13 chr5: 685,748-816,095 , GRCh38.p12 chr5: 685,633-815,980	ZDHHC11B, , 4 more genes
nsv893229	copy number variation	6	nstd71	human		NCBI36 chr9: 43,570,503-43,938,466 , GRCh37.p13 chr9: 43,630,507-43,998,470 , GRCh38.p12 chr9: 41,912,139-42,974,549	LOC100419693, ANKRD20A7P, 30 more genes
nsv897377	copy number variation	19	nstd71	human		NCBI36 chr11: 48,680,611-48,749,266 , GRCh37.p13 chr11: 48,724,035-48,792,690 , GRCh38.p12 chr11: 48,702,483-48,771,138	0

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