1-0690-003 AND nstd173 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4377994	copy number variation	31	nstd173	human		GRCh37 chr1: 72,773,260-72,811,084 , GRCh38.p12 chr1: 72,307,577-72,345,401 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-66,626	LOC105378797
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
nsv4382597	copy number variation	1	nstd173	human		GRCh37 chr4: 15,693,245-15,726,910 , GRCh38.p12 chr4: 15,691,622-15,725,287	BST1
nsv4370644	copy number variation	1	nstd173	human		GRCh37 chr12: 11,497,999-11,553,849 , GRCh38.p12 chr12: 11,345,065-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 540,028-572,349	PRB2, PRB1
nsv4376451	copy number variation	1	nstd173	human		GRCh37 chr8: 2,127,154-2,179,661 , GRCh38.p12 chr8: 2,178,951-2,231,994 , GRCh38.p12 chr8\|NT_187576.1: 362,364-414,871	LOC105377781, LOC105377782
nsv4367277	copy number variation	1	nstd173	human		GRCh37 chr8: 2,347,503-2,596,106 , GRCh38.p12 chr8: 2,605,460-2,738,578 , GRCh38.p12 chr8\|NT_187576.1: 658,073-809,178	LOC107986865, LINC03021
nsv4383109	copy number variation	49	nstd173	human		GRCh37 chr11: 55,374,031-55,453,575 , GRCh38.p12 chr11: 55,606,555-55,686,099	OR4P1P, OR4P4, 3 more genes
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4386129	copy number variation	134	nstd173	human		GRCh37 chr17: 34,439,977-34,477,480 , GRCh38.p12 chr17: 36,112,584-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,681-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,505-385,008	LOC101927369, LOC100419980, 2 more genes
nsv4387150	copy number variation	27	nstd173	human		GRCh37 chr19: 24,378,991-24,419,660 , GRCh38.p12 chr19: 24,196,189-24,236,858	0
nsv4384312	copy number variation	11	nstd173	human		GRCh37 chr10: 46,966,534-48,006,310 , GRCh38.p12 chr10: 46,157,935-47,923,579	RN7SL453P, ANTXRLP1, 54 more genes
nsv4379969	copy number variation	9	nstd173	human		GRCh37 chr14: 22,586,012-22,959,555 , GRCh38.p12 chr14: 22,118,059-22,490,567	TRAV36DV7, TRDD3, 47 more genes
nsv4387566	copy number variation	315	nstd173	human		GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0

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