215691 AND nstd173 - dbVar - NCBI

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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
nsv4386852	copy number variation	127	nstd173	human		GRCh37 chr8: 137,677,896-137,862,435 , GRCh38.p12 chr8: 136,665,653-136,850,192	LINC02055
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4379432	copy number variation	10	nstd173	human		GRCh37 chr2: 130,817,326-130,863,844 , GRCh38.p12 chr2: 130,059,753-130,106,271	POTEF, POTEF-AS1
nsv4383020	copy number variation	1	nstd173	human		GRCh37 chrX: 79,893,291-80,011,045 , GRCh38.p12 chrX: 80,637,792-80,755,546	PSMA1P1, BRWD3
nsv4365700	copy number variation	12	nstd173	human		GRCh37 chr19: 52,131,734-52,154,905 , GRCh38.p12 chr19: 51,628,481-51,651,652	SIGLEC5, SIGLEC14, 1 more genes
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4370631	copy number variation	136	nstd173	human		GRCh37 chr11: 5,787,573-5,809,230 , GRCh38.p12 chr11: 5,766,343-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4369134	copy number variation	12	nstd173	human		GRCh37 chr12: 19,467,159-19,577,135 , GRCh38.p12 chr12: 19,314,225-19,424,201	PLEKHA5, PDCD5P1, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4385346	copy number variation	1	nstd173	human		GRCh37 chr1: 196,716,413-196,913,251 , GRCh38.p12 chr1: 196,747,283-196,944,121	CFH, CFHR1, 5 more genes
nsv4386668	copy number variation	1	nstd173	human		GRCh37 chr7: 63,530,076-63,796,210 , GRCh38.p12 chr7: 64,069,698-64,335,832	VN1R39P, MTND4P2, 21 more genes
nsv4381249	copy number variation	16	nstd173	human		GRCh37 chr3: 98,936,926-98,964,849 , GRCh38.p12 chr3: 99,218,082-99,246,005	0
nsv4372688	copy number variation	4	nstd173	human		GRCh37 chr6: 168,336,556-168,583,576 , GRCh38.p12 chr6: 167,935,876-168,182,896	HGC6.3, LOC107986673, 6 more genes
nsv4373366	copy number variation	7	nstd173	human		GRCh37 chr7: 38,322,939-38,370,792 , GRCh38.p12 chr7: 38,283,338-38,331,191	TRGV9, TRG, 7 more genes
nsv4373107	copy number variation	1	nstd173	human		GRCh37 chr16: 29,654,589-30,177,240 , GRCh38.p12 chr16: 29,643,268-30,165,919	MVP-DT, MAPK3, 32 more genes
nsv4381843	copy number variation	2	nstd173	human		GRCh37 chr14: 22,533,752-22,974,116 , GRCh38.p12 chr14: 22,065,488-22,505,130	TRAJ39, TRAV35, 65 more genes

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