10-0014-001 AND nstd173 - dbVar - NCBI

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Items: 15

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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
nsv4375488	copy number variation	51	nstd173	human		GRCh37 chr1: 196,714,810-196,741,354 , GRCh38.p12 chr1: 196,745,680-196,772,224	CFH
nsv4381799	copy number variation	5	nstd173	human		GRCh37 chr2: 98,141,311-98,161,709 , GRCh38.p12 chr2: 97,524,848-97,545,246	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
nsv4381433	copy number variation	68	nstd173	human		GRCh37 chr1: 196,827,842-196,877,049 , GRCh38.p12 chr1: 196,858,712-196,907,919	LOC100996886, CFHR4
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
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4369049	copy number variation	64	nstd173	human		GRCh37 chr12: 8,004,412-8,124,048 , GRCh38.p12 chr12: 7,851,816-7,971,452	NANOGP1, SLC2A14, 3 more genes
nsv4385449	copy number variation	2	nstd173	human		GRCh37 chr12: 19,467,159-19,576,237 , GRCh38.p12 chr12: 19,314,225-19,423,303	PDCD5P1, AEBP2, 1 more genes
nsv4379624	copy number variation	3	nstd173	human		GRCh37 chr14: 22,441,153-22,995,123 , GRCh38.p12 chr14: 21,972,924-22,526,154	TRAJ55, TRAV28, 91 more genes
nsv4370124	copy number variation	182	nstd173	human		GRCh37 chr7: 142,266,307-142,493,638 , GRCh38.p12 chr7: 142,618,685-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, TRBV21-1, 23 more genes
nsv4374869	copy number variation	45	nstd173	human		GRCh37 chr7: 38,295,932-38,394,857 , GRCh38.p12 chr7: 38,256,331-38,355,256	TRGVA, , 19 more genes
nsv4384859	copy number variation	4	nstd173	human		GRCh37 chr3: 8,825,346-8,856,526 , GRCh38.p12 chr3: 8,783,660-8,814,840	0
nsv4388385	copy number variation	148	nstd173	human		GRCh37 chr14: 106,537,003-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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