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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3827587copy number variation1estd219human GRCh37 chr2: 193,988,581-194,086,760 , GRCh38.p12 chr2: 193,123,855-193,222,034 LOC107985969
    esv3834770copy number variation743estd219human 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
    esv3850922copy number variation9estd219human GRCh37 chr7: 111,095,114-111,159,260 , GRCh38.p12 chr7: 111,455,058-111,519,204 IMMP2L
    esv3834769copy number variation743estd219human 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
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3824832copy number variation42estd219human GRCh37 chr2: 73,875,648-73,913,665 , GRCh38.p12 chr2: 73,648,521-73,686,538 ALMS1P1
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3850906copy number variation15estd219human GRCh37 chr7: 110,993,965-111,025,274 , GRCh38.p12 chr7: 111,353,909-111,385,218 IMMP2L
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3851668copy number variation544estd219human GRCh37 chr7: 141,765,307-141,792,849 , GRCh38.p12 chr7|NT_187562.1: 27,387-54,929 , GRCh38.p12 chr7: 142,065,507-142,093,049 MGAM
    esv3827608copy number variation40estd219human GRCh37 chr2: 194,577,966-194,601,084 , GRCh38.p12 chr2: 193,713,242-193,736,360 SEC61GP1
    esv3850909copy number variation15estd219human GRCh37 chr7: 111,024,794-111,042,522 , GRCh38.p12 chr7: 111,384,738-111,402,466 IMMP2L
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3836299copy number variation94estd219human GRCh37 chr4: 98,172,077-98,187,731 , GRCh38.p12 chr4: 97,250,926-97,266,580 STPG2
    esv3833727copy number variation624estd219human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 MUC20
    esv3850618copy number variation797estd219human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3839320copy number variation103estd219human GRCh37 chr5: 17,639,160-17,651,755 , GRCh38.p12 chr5: 17,639,051-17,651,646 LOC391768
    esv3865261copy number variation38estd219human GRCh37 chr11: 99,646,049-99,660,450 , GRCh38.p12 chr11: 99,775,318-99,789,719 CNTN5
    esv3886329copy number variation610estd219human GRCh37 chr21: 23,653,294-23,667,590 , GRCh38.p12 chr21|NW_003315968.2: 185,203-199,499 , GRCh38.p12 chr21: 22,280,974-22,295,270 LOC107985508
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