SP50148 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
nsv901838	copy number variation	1	nstd71	human		NCBI36 chr14: 44,138,999-44,366,800 , GRCh37.p13 chr14: 45,069,249-45,297,050 , GRCh38.p12 chr14: 44,600,046-44,827,847	LINC02302
nsv872401	copy number variation	7	nstd71	human		NCBI36 chr1: 147,710,728-147,856,593 , GRCh37.p13 chr1: 149,444,104-149,589,969 , GRCh38.p12 chr1: 120,852,223-120,926,682	LINC00623, PPIAL4A, 1 more genes
nsv879345	copy number variation	351	nstd71	human		NCBI36 chr4: 69,117,497-69,179,871 , GRCh37.p13 chr4: 69,434,902-69,497,276 , GRCh38.p12 chr4: 68,569,184-68,631,558	UGT2B17, LOC100132651, 2 more genes
nsv880916	copy number variation	3	nstd71	human		NCBI36 chr5: 786,926-847,224 , GRCh37.p13 chr5: 733,926-794,224 , GRCh38.p12 chr5: 733,811-794,109	ZDHHC11, ZDHHC11B, 1 more genes
nsv888236	copy number variation	11	nstd71	human		NCBI36 chr7: 62,499,511-62,559,231 , GRCh37.p13 chr7: 62,862,076-62,921,796 , GRCh38.p12 chr7: 63,401,698-63,461,418	ARAFP2, ZNF734P, 1 more genes
nsv905370	copy number variation	14	nstd71	human		NCBI36 chr16: 14,948,604-15,032,942 , GRCh37.p13 chr16: 15,041,103-15,125,441 , GRCh38.p12 chr16: 14,947,246-15,031,584	LOC728138, PKD1P3-NPIPA1, 3 more genes
nsv882124	copy number variation	1	nstd71	human		NCBI36 chr5: 70,307,261-70,434,279 , GRCh37.p13 chr5: 70,271,505-70,398,523 , GRCh38.p12 chr5: 70,975,678-71,102,696	OCLNP1, NAIPP4, 4 more genes
nsv901418	copy number variation	1	nstd71	human		NCBI36 chr14: 19,365,350-19,473,931 , GRCh37.p13 chr14: 20,295,510-20,404,091 , GRCh38.p12 chr14: 19,827,351-19,935,932	OR4N2, OR4K4P, 6 more genes
nsv904048	copy number variation	34	nstd71	human		NCBI36 chr15: 32,509,924-32,606,592 , GRCh37.p13 chr15: 34,722,632-34,819,300 , GRCh38.p12 chr15: 34,430,431-34,527,099	DNM1P5, FSCN1P1, 4 more genes
nsv872313	copy number variation	5	nstd71	human		NCBI36 chr1: 147,292,384-147,503,683 , GRCh37.p13 chr1: 149,025,760-149,237,059 , GRCh38.p12 chr1: 143,531,138-143,742,404	TRN-GTT22-1, TRQ-CTG4-2, 10 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
nsv902575	copy number variation	2	nstd71	human		NCBI36 chr14: 105,161,788-105,224,179 , GRCh37.p13 chr14: 106,090,743-106,153,134 , GRCh37.p13 chr14\|NW_004166863.1: 287,573-349,964 , GRCh38.p12 chr14: 105,624,406-105,686,797 , GRCh38.p12 chr14\|NT_187600.1: 92,175-154,566	ELK2AP, , 7 more genes
nsv908106	copy number variation	11	nstd71	human		NCBI36 chr17: 31,460,821-31,511,943 , GRCh37.p13 chr17: 34,442,621-34,487,830 , GRCh37.p13 chr17\|NW_003315949.1: 1-45,210 , GRCh38.p12 chr17: 36,109,315-36,160,457 , GRCh38.p12 chr17\|NT_187614.1: 344,236-395,358 , GRCh38.p12 chr17\|NT_187661.1: 63,412-114,553	, LOC100419980, 4 more genes

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