229190S AND nstd173 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4382938	copy number variation	14	nstd173	human		GRCh37 chr20: 1,560,530-1,597,997 , GRCh38.p12 chr20: 1,579,884-1,617,351	SIRPB1
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4376877	copy number variation	6	nstd173	human		GRCh37 chr16: 60,549,016-60,575,074 , GRCh38.p12 chr16: 60,515,112-60,541,170	LOC101927605
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4370075	copy number variation	1	nstd173	human		GRCh37 chr7: 153,821,453-154,217,178 , GRCh38.p12 chr7: 154,124,368-154,520,093	DPP6, LOC105375582
nsv4375526	copy number variation	1	nstd173	human		GRCh37 chr16: 63,096,916-63,199,107 , GRCh38.p12 chr16: 63,063,012-63,165,203	LOC105371307, LOC105371308
nsv4376113	copy number variation	7	nstd173	human		GRCh37 chr1: 1,397,490-1,429,163 , GRCh38.p12 chr1: 1,462,110-1,493,783	ATAD3B, ATAD3C
nsv4379784	copy number variation	3	nstd173	human		GRCh37 chr13: 64,345,818-64,387,689 , GRCh38.p12 chr13: 63,771,685-63,813,556	PPP1R2P10, RNU6-81P
nsv4388035	copy number variation	283	nstd173	human		GRCh37 chr1: 104,109,088-104,132,506 , GRCh38.p12 chr1: 103,566,466-103,589,884	AMY2B, ACTG1P4
nsv4368257	copy number variation	154	nstd173	human		GRCh37 chr11: 55,374,147-55,453,008 , GRCh38.p12 chr11: 55,606,671-55,685,532	OR4V1P, OR4P1P, 3 more genes
nsv4381596	copy number variation	144	nstd173	human		GRCh37 chr14: 74,001,123-74,024,031 , GRCh38.p12 chr14: 73,534,419-73,557,327	HEATR4, NT5CP2, 1 more genes
nsv4380085	copy number variation	1	nstd173	human		GRCh37 chr22: 47,775,871-47,835,357 , GRCh38.p12 chr22: 47,380,121-47,439,607	0
nsv4382592	copy number variation	3	nstd173	human		GRCh37 chr14: 45,182,148-45,227,365 , GRCh38.p12 chr14: 44,712,945-44,758,162	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4369957	copy number variation	137	nstd173	human		GRCh37 chr10: 46,966,546-47,149,423 , GRCh38.p12 chr10: 46,400,340-46,583,071	GPRIN2, , 5 more genes
nsv4367728	copy number variation	10	nstd173	human		GRCh37 chr14: 22,410,620-22,978,349 , GRCh38.p12 chr14: 21,942,429-22,509,365	TRAV8-6, TRAJ52, 79 more genes
nsv4366216	copy number variation	3	nstd173	human		GRCh37 chr7: 142,254,561-142,475,287 , GRCh38.p12 chr7: 142,618,685-142,732,123 , GRCh38.p12 chr7\|NT_187562.1: 656,734-770,033	TRBV27, TRBV24-1, 16 more genes
nsv4380231	copy number variation	12	nstd173	human		GRCh37 chr7: 38,319,296-38,405,084 , GRCh38.p12 chr7: 38,279,695-38,365,483	TRGVB, TRGV10, 15 more genes
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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