SAMN00009105 AND estd214 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
esv3605891	copy number variation	49	estd214	human	GRCh37 chr5: 97,050,505-97,128,253 , GRCh38.p12 chr5: 97,714,801-97,792,549	LOC391813
esv3605892	copy number variation	40	estd214	human	GRCh37 chr5: 97,049,822-97,126,058 , GRCh38.p12 chr5: 97,714,118-97,790,354	LOC391813
esv3600181	copy number variation	743	estd214	human	GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4: 34,779,695-34,848,264 , GRCh38.p12 chr4\|NW_003315915.1: 272,024-340,593	LOC105378262
esv3634197	copy number variation	646	estd214	human	GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445	LINC02315
esv3616948	copy number variation	1095	estd214	human	GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804	ADAM5
esv3600180	copy number variation	743	estd214	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
esv3605890	copy number variation	54	estd214	human	GRCh37 chr5: 97,047,859-97,096,156 , GRCh38.p12 chr5: 97,712,155-97,760,452	LOC391813
esv3587491	copy number variation	2473	estd214	human	GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198	PPIAL4A
esv3596597	copy number variation	82	estd214	human	GRCh37 chr3: 75,423,550-75,458,952 , GRCh38.p12 chr3: 75,374,399-75,409,801	LSP1P2
esv3644983	copy number variation	2409	estd214	human	GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039	SIRPB1
esv3623922	copy number variation	1739	estd214	human	GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640	NUTM2B-AS1
esv3632602	copy number variation	198	estd214	human	GRCh37 chr13: 69,244,390-69,269,055 , GRCh38.p12 chr13: 68,670,258-68,694,923	RN7SL761P
esv3638686	copy number variation	852	estd214	human	GRCh37 chr16: 55,798,890-55,822,423 , GRCh38.p12 chr16: 55,764,978-55,788,511	CES1P1
esv3603772	copy number variation	1611	estd214	human	GRCh37 chr5: 757,676-778,933 , GRCh38.p12 chr5: 757,561-778,818	ZDHHC11B
esv3591709	copy number variation	1476	estd214	human	GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104	ANKRD36B
esv3587880	copy number variation	879	estd214	human	GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586	NME7
esv3628470	copy number variation	4908	estd214	human	GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431	OR7E148P
esv3593502	copy number variation	1244	estd214	human	GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292	SESTD1
esv3588654	copy number variation	11	estd214	human	GRCh37 chr1: 206,315,586-206,332,640 , GRCh38.p12 chr1: 206,008,728-206,025,782	CTSE
esv3615872	copy number variation	601	estd214	human	GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8\|NT_187576.1: 485,727-501,813	LOC105377783

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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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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 2575

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Number of Variants: 20

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