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Items: 1 to 20 of 3156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    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
    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
    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
    esv3882202copy number variation3estd219human GRCh37 chr18: 64,726,676-64,754,058 , GRCh38.p12 chr18: 67,059,439-67,086,821 MIR5011
    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
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    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
    esv3879060copy number variation208estd219human GRCh37 chr17: 15,042,705-15,059,719 , GRCh38.p12 chr17: 15,139,388-15,156,402 LOC107984976
    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
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3850618copy number variation797estd219human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3820413copy number variation357estd219human GRCh37 chr1: 111,376,500-111,388,793 , GRCh38.p12 chr1: 110,833,878-110,846,171 NRBF2P3
    esv3868353copy number variation3estd219human GRCh37 chr12: 87,020,513-87,032,539 , GRCh38.p12 chr12: 86,626,736-86,638,762 MGAT4C
    esv3864936copy number variation232estd219human GRCh37 chr11: 89,798,932-89,810,560 , GRCh38.p12 chr11: 90,065,764-90,077,392 TRIM49C
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