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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4114981copy number variation1nstd166human GRCh37.p13 chr5: 134,904,496-134,904,557 , GRCh38.p12 chr5: 135,568,806-135,568,867 CXCL14
    esv3566679copy number variation1estd215human GRCh37 chr5: 134,907,432-134,907,455 , GRCh38.p12 chr5: 135,571,742-135,571,765 CXCL14
    esv2472290copy number variation1estd197human NCBI36 chr5: 134,936,640-134,936,640 , GRCh37.p13 chr5: 134,908,741-134,908,741 , GRCh38.p12 chr5: 135,573,051-135,573,051 CXCL14
    esv2159845copy number variation1estd194human NCBI36 chr5: 134,936,631-134,936,632 , GRCh37.p13 chr5: 134,908,732-134,908,733 , GRCh38.p12 chr5: 135,573,042-135,573,043 CXCL14
    esv1637026copy number variation1estd22human NCBI36 chr5: 134,935,351-134,935,374 , GRCh37.p13 chr5: 134,907,452-134,907,475 , GRCh38.p12 chr5: 135,571,762-135,571,785 CXCL14
    esv1044691copy number variation1estd22human NCBI36 chr5: 134,937,329-134,937,331 , GRCh37.p13 chr5: 134,909,430-134,909,432 , GRCh38.p12 chr5: 135,573,740-135,573,742 CXCL14
    nsv327160copy number variation1nstd6human NCBI35 chr5: 134,935,352-134,935,374 , GRCh37.p13 chr5: 134,907,453-134,907,475 , GRCh38.p12 chr5: 135,571,763-135,571,785 CXCL14
    nsv2370786short tandem repeat10nstd128human GRCh37 chr5: 134,909,400-134,909,432 , GRCh38.p12 chr5: 135,573,710-135,573,742 CXCL14
    nsv2371078short tandem repeat1nstd128human GRCh37 chr5: 134,905,455-134,905,483 , GRCh38.p12 chr5: 135,569,765-135,569,793 CXCL14
    nsv2373718short tandem repeat2nstd128human GRCh37 chr5: 134,904,533-134,904,555 , GRCh38.p12 chr5: 135,568,843-135,568,865 CXCL14
    nsv2370785short tandem repeat1nstd128human GRCh37 chr5: 134,908,514-134,908,532 , GRCh38.p12 chr5: 135,572,824-135,572,842 CXCL14
    nsv6793305copy number variation1nstd229human GRCh38 chr5: 135,574,685-135,578,433 , GRCh37.p13 chr5: 134,910,375-134,914,123 SLC25A48, CXCL14
    nsv3125460copy number variation1nstd151human GRCh37 chr5: 134,907,540-134,914,234 , GRCh38.p12 chr5: 135,571,850-135,578,544 CXCL14, SLC25A48
    nsv2370787short tandem repeat1nstd128human GRCh37 chr5: 134,914,430-134,914,448 , GRCh38.p12 chr5: 135,578,740-135,578,758 CXCL14, SLC25A48
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 TXNDC15, PCDHAC1, 962 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 more genes
    nsv3920627copy number variation1nstd102humanPathogenic NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694 MIR1289-2, DCANP1, 138 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv3919979copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626 FBXL21P, MIR5692C1, 92 more genes
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