HG01871 AND estd219 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
esv3837861	copy number variation	1	estd219	human	GRCh37 chr4: 161,118,946-161,227,781 , GRCh38.p12 chr4: 160,197,794-160,306,629	LOC107986239
esv3834770	copy number variation	743	estd219	human	GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4\|NW_003315915.1: 272,024-340,593 , GRCh38.p12 chr4: 34,779,695-34,848,264	LOC105378262
esv3872670	copy number variation	646	estd219	human	GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445	LINC02315
esv3834769	copy number variation	743	estd219	human	GRCh37 chr4: 34,779,933-34,828,997 , GRCh38.p12 chr4\|NW_003315915.1: 270,640-319,704 , GRCh38.p12 chr4: 34,778,311-34,827,375	LOC105378262
esv3820750	copy number variation	2473	estd219	human	GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198	PPIAL4A
esv3840050	copy number variation	21	estd219	human	GRCh37 chr5: 41,564,154-41,600,321 , GRCh38.p12 chr5: 41,564,052-41,600,219	TCP1P2
esv3884482	copy number variation	2409	estd219	human	GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039	SIRPB1
esv3835569	copy number variation	1672	estd219	human	GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335	UGT2B17
esv3828167	copy number variation	1	estd219	human	GRCh37 chr2: 217,676,582-217,705,292 , GRCh38.p12 chr2: 216,811,859-216,840,569	IGFBP-AS1
esv3821155	copy number variation	879	estd219	human	GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586	NME7
esv3849507	copy number variation	27	estd219	human	GRCh37 chr7: 56,804,315-56,822,416 , GRCh38.p12 chr7: 56,736,622-56,754,723	LOC728416
esv3887266	copy number variation	12	estd219	human	GRCh37 chr22: 28,591,562-28,611,552 , GRCh38.p12 chr22: 28,195,574-28,215,564	TTC28
esv3827261	copy number variation	1244	estd219	human	GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292	SESTD1
esv3858600	copy number variation	527	estd219	human	GRCh37 chr9: 113,024,583-113,037,085 , GRCh38.p12 chr9: 110,262,303-110,274,805	LOC107987114
esv3890498	copy number variation	1565	estd219	human	GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709	TMLHE
esv3875253	copy number variation	292	estd219	human	GRCh37 chr15: 56,789,510-56,801,390 , GRCh38.p12 chr15: 56,497,312-56,509,192
esv3840053	copy number variation	17	estd219	human	GRCh37 chr5: 41,585,697-41,596,432 , GRCh38.p12 chr5: 41,585,595-41,596,330	TCP1P2
esv3835105	copy number variation	4	estd219	human	GRCh37 chr4: 48,710,635-48,722,063 , GRCh38.p12 chr4: 48,708,618-48,720,046	FRYL
esv3867268	copy number variation	6	estd219	human	GRCh37 chr12: 40,446,318-40,456,457 , GRCh38.p12 chr12: 40,052,516-40,062,655	SLC2A13
esv3833638	copy number variation	2212	estd219	human	GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766	VEZF1P1

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 3244

Page of 163

Number of Variants: 20

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