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Items: 1 to 20 of 3648

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3875848copy number variation139estd219human GRCh37 chr15: 86,064,810-86,182,627 , GRCh38.p12 chr15: 85,521,579-85,639,396 AKAP13
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3828809copy number variation58estd219human GRCh37 chr2: 242,852,906-242,902,712 , GRCh38.p12 chr2: 241,910,755-241,960,561 , GRCh38.p12 chr2|NT_187527.1: 122,853-173,422 LINC01237
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3826258copy number variation31estd219human GRCh37 chr2: 138,038,871-138,073,811 , GRCh38.p12 chr2: 137,281,301-137,316,241 THSD7B
    esv3846437copy number variation7estd219human GRCh37 chr6: 119,531,666-119,566,950 , GRCh38.p12 chr6: 119,210,501-119,245,785 MAN1A1
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3828811copy number variation67estd219human GRCh37 chr2: 242,860,074-242,892,607 , GRCh38.p12 chr2|NT_187527.1: 130,021-163,317 , GRCh38.p12 chr2: 241,917,923-241,950,456 LINC01237
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3828808copy number variation67estd219human GRCh37 chr2: 242,850,168-242,875,365 , GRCh38.p12 chr2|NT_187527.1: 120,115-146,085 , GRCh38.p12 chr2: 241,908,017-241,933,214 LINC01237
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3821978copy number variation11estd219human GRCh37 chr1: 206,315,586-206,332,640 , GRCh38.p12 chr1: 206,008,728-206,025,782 CTSE
    esv3852311copy number variation601estd219human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3836524copy number variation1estd219human GRCh37 chr4: 107,660,872-107,676,607 , GRCh38.p12 chr4: 106,739,715-106,755,450 LOC105377356
    esv3828822copy number variation78estd219human GRCh37 chr2: 242,950,776-242,961,450 , GRCh38.p12 chr2: 242,008,625-242,019,299 , GRCh38.p12 chr2|NT_187647.1: 47,254-62,395 , GRCh38.p12 chr2|NT_187523.1: 47,320-63,369 LINC01237
    esv3828812copy number variation67estd219human GRCh37 chr2: 242,881,801-242,896,363 , GRCh38.p12 chr2: 241,939,650-241,954,212 , GRCh38.p12 chr2|NT_187527.1: 152,521-167,073 LINC01237
    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
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3870250copy number variation7estd219human GRCh37 chr13: 47,449,872-47,463,783 , GRCh38.p12 chr13: 46,875,737-46,889,648 HTR2A
    esv3858600copy number variation527estd219human GRCh37 chr9: 113,024,583-113,037,085 , GRCh38.p12 chr9: 110,262,303-110,274,805 LOC107987114
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