1-0139-004 AND nstd173 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv4373339	copy number variation	53	nstd173	human		GRCh37 chrX: 150,698,534-150,722,241 , GRCh38.p12 chrX: 151,530,062-151,553,769	LOC105373367
nsv4375641	copy number variation	3	nstd173	human		GRCh37 chrX: 32,999,487-33,020,261 , GRCh38.p12 chrX: 32,981,370-33,002,144	DMD
nsv4368434	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,366-72,812,440 , GRCh38.p12 chr1: 72,305,683-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,982	LOC105378797
nsv4382870	copy number variation	4	nstd173	human		GRCh37 chr3: 87,947,013-88,007,774 , GRCh38.p12 chr3: 87,897,863-87,958,624	RNU6ATAC6P, HTR1F
nsv4386519	copy number variation	35	nstd173	human		GRCh37 chr8: 39,246,772-39,389,002 , GRCh38.p12 chr8: 39,389,253-39,531,483	ADAM3A, ADAM5
nsv4384457	copy number variation	635	nstd173	human		GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 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
nsv4378105	copy number variation	17	nstd173	human		GRCh37 chr5: 177,227,228-177,250,458 , GRCh38.p12 chr5: 177,800,227-177,823,457	, , 1 more genes
nsv4365684	copy number variation	5	nstd173	human		GRCh37 chr1: 195,823,043-195,876,205 , GRCh38.p12 chr1: 195,853,913-195,907,075	0
nsv4383295	copy number variation	43	nstd173	human		GRCh37 chr5: 46,106,822-46,136,706 , GRCh38.p12 chr5: 46,106,720-46,136,604	0
nsv4370854	copy number variation	55	nstd173	human		GRCh37 chr6: 31,280,867-31,305,152 , GRCh38.p12 chr6: 31,313,090-31,337,375	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
nsv4386199	copy number variation	21	nstd173	human		GRCh37 chr22: 22,311,349-22,578,983 , GRCh38.p12 chr22: 21,956,977-22,224,590	IGLV4-69, IGLV10-54, 27 more genes
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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