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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890872copy number variation1nstd102humanBenign GRCh37 chr19: 517,392-529,004 , GRCh38.p12 chr19: 517,392-529,004 TPGS1
    nsv3905385copy number variation1nstd102humanBenign GRCh37 chr19: 509,569-518,897 , GRCh38.p12 chr19: 509,569-518,897 TPGS1
    nsv3891112copy number variation1nstd102humanBenign GRCh37 chr19: 517,336-525,739 , GRCh38.p12 chr19: 517,336-525,739 TPGS1
    nsv3899561copy number variation1nstd102humanBenign GRCh37 chr19: 517,284-541,260 , GRCh38.p12 chr19: 517,284-541,260 TPGS1, CDC34
    nsv3894495copy number variation1nstd102humanBenign GRCh37 chr19: 517,392-541,260 , GRCh38.p12 chr19: 517,392-541,260 TPGS1, CDC34
    nsv3896665copy number variation1nstd102humanBenign GRCh37 chr19: 517,336-540,727 , GRCh38.p12 chr19: 517,336-540,727 TPGS1, CDC34
    nsv3894810copy number variation1nstd102humanBenign GRCh37 chr19: 517,392-540,727 , GRCh38.p12 chr19: 517,392-540,727 TPGS1, CDC34
    nsv3904631copy number variation1nstd102humanBenign GRCh37 chr19: 496,724-529,004 , GRCh38.p12 chr19: 496,724-529,004 TPGS1, MADCAM1, 1 more genes
    nsv3905884copy number variation1nstd102humanBenign GRCh37 chr19: 499,978-529,004 , GRCh38.p12 chr19: 499,978-529,004 TPGS1, MADCAM1, 1 more genes
    nsv3903889copy number variation1nstd102humanBenign GRCh37 chr19: 474,588-541,685 , GRCh38.p12 chr19: 474,588-541,685 TPGS1, CDC34, 3 more genes
    nsv3898347copy number variation1nstd102humanLikely benign GRCh37 chr19: 467,701-519,619 , GRCh38.p12 chr19: 467,701-519,619 TPGS1, CIMAP1D, 2 more genes
    nsv3898580copy number variation1nstd102humanBenign GRCh37 chr19: 460,883-512,568 , GRCh38.p12 chr19: 460,883-512,568 TPGS1, CIMAP1D, 3 more genes
    nsv3894779copy number variation1nstd102humanBenign GRCh37 chr19: 474,588-525,739 , GRCh38.p12 chr19: 474,588-525,739 TPGS1, CIMAP1D, 2 more genes
    nsv3895601copy number variation1nstd102humanLikely benign GRCh37 chr19: 474,645-519,619 , GRCh38.p12 chr19: 474,645-519,619 TPGS1, MADCAM1, 2 more genes
    nsv3908727copy number variation1nstd102humanBenign GRCh37 chr19: 474,588-518,841 , GRCh38.p12 chr19: 474,588-518,841 TPGS1, CIMAP1D, 2 more genes
    nsv3894677copy number variation1nstd102humanBenign GRCh37 chr19: 473,932-517,284 , GRCh38.p12 chr19: 473,932-517,284 TPGS1, CIMAP1D, 2 more genes
    nsv3909604copy number variation1nstd102humanBenign GRCh37 chr19: 474,645-509,267 , GRCh38.p12 chr19: 474,645-509,267 TPGS1, MADCAM1, 2 more genes
    nsv3906850copy number variation1nstd102humanBenign GRCh37 chr19: 474,645-508,220 , GRCh38.p12 chr19: 474,645-508,220 TPGS1, MADCAM1, 2 more genes
    nsv3898649copy number variation1nstd102humanBenign GRCh37 chr19: 478,060-508,626 , GRCh38.p12 chr19: 478,060-508,626 TPGS1, CIMAP1D, 2 more genes
    nsv3895626copy number variation1nstd102humanBenign GRCh37 chr19: 495,722-525,739 , GRCh38.p12 chr19: 495,722-525,739 TPGS1, MADCAM1, 1 more genes
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