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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2665317copy number variation65estd199human GRCh37 chr11: 7,811,173-7,833,378 , GRCh38.p12 chr11: 7,789,626-7,811,831 , GRCh38.p12 chr11|NT_187583.1: 10,494-32,699 , GRCh38.p12 chr11|NW_011332695.1: 10,494-32,701 OR5P2
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2663931copy number variation243estd199human GRCh37 chr4: 138,092,000-138,100,631 , GRCh38.p12 chr4: 137,170,846-137,179,477 LINC02511
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    esv2658993copy number variation297estd199human GRCh37 chr8: 51,031,091-51,038,329 , GRCh38.p12 chr8: 50,118,531-50,125,769 SNTG1
    esv2673118copy number variation530estd199human GRCh37 chr6: 136,582,615-136,589,299 , GRCh38.p12 chr6: 136,261,477-136,268,161 BCLAF1
    esv2676602copy number variation220estd199human GRCh37 chr3: 197,843,926-197,850,166 , GRCh38.p12 chr3: 198,117,055-198,123,295 , GRCh38.p12 chr3|NT_187539.1: 112,264-118,563 TUBB8P8
    esv2665467copy number variation213estd199human GRCh37 chr4: 88,268,243-88,274,298 , GRCh38.p12 chr4: 87,347,091-87,353,146 HSD17B11
    esv2661148copy number variation777estd199human GRCh37 chr15: 83,551,620-83,557,670 , GRCh38.p12 chr15: 82,882,868-82,888,918 HOMER2
    esv2656476copy number variation583estd199human GRCh37 chr5: 108,595,074-108,601,121 , GRCh38.p12 chr5: 109,259,373-109,265,420 LOC285638
    esv2664916copy number variation708estd199human GRCh37 chr4: 167,677,036-167,683,071 , GRCh38.p12 chr4: 166,755,885-166,761,920 SPOCK3
    esv2665281copy number variation795estd199human GRCh37 chr3: 22,092,347-22,097,795 , GRCh38.p12 chr3: 22,050,855-22,056,303 ZNF385D
    esv2677725copy number variation507estd199human GRCh37 chr9: 29,092,574-29,098,014 , GRCh38.p12 chr9: 29,092,576-29,098,016 LINGO2
    esv2674467copy number variation119estd199human GRCh37 chrX: 2,365,760-2,371,100 , GRCh38.p12 chrX: 2,447,719-2,453,059 DHRSX
    esv2662772copy number variation652estd199human GRCh37 chr3: 136,021,013-136,026,199 , GRCh38.p12 chr3: 136,302,171-136,307,357 PCCB
    esv2673283copy number variation717estd199human GRCh37 chr16: 76,539,133-76,544,025 , GRCh38.p12 chr16: 76,505,236-76,510,128 CNTNAP4
    esv2671808copy number variation84estd199human GRCh37 chr8: 3,786,013-3,790,747 , GRCh38.p12 chr8: 3,928,491-3,933,225 CSMD1
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