SAMN00001676 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
esv3621643	copy number variation	4	estd214	human	GRCh37 chr9: 122,841,299-122,890,163 , GRCh38.p12 chr9: 120,079,021-120,127,885
esv3596068	copy number variation	520	estd214	human	GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669	PRSS44P
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
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
esv3632214	copy number variation	1037	estd214	human	GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443	MTCO2P3
esv3588471	copy number variation	1062	estd214	human	GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810	CFHR3
esv3600875	copy number variation	1672	estd214	human	GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335	UGT2B17
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
esv3620473	copy number variation	1254	estd214	human	GRCh37 chr9: 43,580,844-43,606,160 , GRCh38.p12 chr9: 42,208,229-42,233,545	LOC112268036
esv3603772	copy number variation	1611	estd214	human	GRCh37 chr5: 757,676-778,933 , GRCh38.p12 chr5: 757,561-778,818	ZDHHC11B
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
esv3624746	copy number variation	147	estd214	human	GRCh37 chr10: 122,769,702-122,787,504 , GRCh38.p12 chr10: 121,010,189-121,027,991	LOC105378521
esv3623140	copy number variation	1029	estd214	human	GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441	ASAH2
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
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
esv3609614	copy number variation	648	estd214	human	GRCh37 chr6: 77,437,459-77,453,275 , GRCh38.p12 chr6: 76,727,742-76,743,558	LOC105377861
esv3636072	copy number variation	227	estd214	human	GRCh37 chr15: 32,504,287-32,519,739 , GRCh38.p12 chr15: 32,212,086-32,227,538	LOC102724078
esv3614355	copy number variation	206	estd214	human	GRCh37 chr7: 102,351,450-102,367,324 , GRCh38.p12 chr7: 102,711,003-102,726,877	RASA4DP
esv3620460	copy number variation	1877	estd214	human	GRCh37 chr9: 41,971,191-41,985,717 , GRCh38.p12 chr9: 39,826,173-39,840,699	FGF7P3
esv3615090	copy number variation	1169	estd214	human	GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 2796

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Number of Variants: 20

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