HG03479 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
esv3875848	copy number variation	139	estd219	human	GRCh37 chr15: 86,064,810-86,182,627 , GRCh38.p12 chr15: 85,521,579-85,639,396	AKAP13
esv3830173	copy number variation	520	estd219	human	GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669	PRSS44P
esv3826134	copy number variation	99	estd219	human	GRCh37 chr2: 132,764,386-132,807,367 , GRCh38.p12 chr2: 132,006,813-132,049,794	LINC01945
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
esv3862254	copy number variation	270	estd219	human	GRCh37 chr10: 124,338,615-124,378,666 , GRCh38.p12 chr10: 122,579,099-122,619,150	DMBT1
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
esv3870498	copy number variation	1037	estd219	human	GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443	MTCO2P3
esv3821789	copy number variation	1062	estd219	human	GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810	CFHR3
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
esv3842790	copy number variation	95	estd219	human	GRCh37 chr5: 155,566,445-155,591,598 , GRCh38.p12 chr5: 156,139,435-156,164,588	SGCD
esv3849967	copy number variation	159	estd219	human	GRCh37 chr7: 74,537,210-74,561,105 , GRCh38.p12 chr7: 75,121,409-75,145,298	GTF2IRD2B
esv3854325	copy number variation	229	estd219	human	GRCh37 chr8: 75,310,126-75,331,296 , GRCh38.p12 chr8: 74,397,891-74,419,061	GDAP1
esv3860443	copy number variation	1029	estd219	human	GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441	ASAH2
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
esv3852311	copy number variation	601	estd219	human	GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8\|NT_187576.1: 485,727-501,813	LOC105377783
esv3850674	copy number variation	206	estd219	human	GRCh37 chr7: 102,351,450-102,367,324 , GRCh38.p12 chr7: 102,711,003-102,726,877	RASA4DP
esv3827949	copy number variation	23	estd219	human	GRCh37 chr2: 209,232,440-209,248,986 , GRCh38.p12 chr2: 208,367,715-208,384,261	PTH2R
esv3842791	copy number variation	93	estd219	human	GRCh37 chr5: 155,577,187-155,591,410 , GRCh38.p12 chr5: 156,150,177-156,164,400	SGCD
esv3851465	copy number variation	1169	estd219	human	GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
esv3822050	copy number variation	40	estd219	human	GRCh37 chr1: 210,601,313-210,614,176 , GRCh38.p12 chr1\|NW_011332687.1: 207,711-220,574 , GRCh38.p12 chr1: 210,427,969-210,440,832	HHAT

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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 3802

Page of 191

Number of Variants: 20

Page of 191

Supplemental Content

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