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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3092495mobile element insertion1nstd144human GRCh37 (hg19) chr14: 75,914,950-75,914,950 , GRCh38 (hg38) chr14: 75,448,247-75,448,247 JDP2
    nsv2778741copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr14: 62,493,932-107,285,437 , GRCh38 (hg38) chr14: 62,027,214-106,877,229 , NCBI36 (hg18) chr14: 61,563,685-106,356,482 JDP2, SERPINA3, 1094 more genes
    nsv2778054copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr14: 19,794,561-107,234,280 , GRCh38 (hg38) chr14: 18,862,646-106,826,050 , NCBI36 (hg18) chr14: 18,864,561-106,305,325 JDP2, ARF6, 2039 more genes
    nsv2774779copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr14: 73,750,741-107,285,437 , GRCh38 (hg38) chr14: 73,284,033-106,877,229 , NCBI36 (hg18) chr14: 72,820,494-106,356,482 JDP2, SEL1L, 892 more genes
    nsv2773993copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr14: 20,511,672-107,285,437 , GRCh38 (hg38) chr14: 20,043,513-106,877,229 , NCBI36 (hg18) chr14: 19,581,512-106,356,482 JDP2, ARF6, 1991 more genes
    nsv2773617copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr14: 75,575,546-78,941,706 , GRCh38 (hg38) chr14: 75,108,843-78,475,363 , NCBI36 (hg18) chr14: 74,645,299-78,011,459 JDP2, BATF, 75 more genes
    nsv1773030short tandem repeat3nstd128human GRCh37 (hg19) chr14: 75,910,269-75,910,279 , GRCh38 (hg38) chr14: 75,443,566-75,443,576 JDP2
    nsv1773029short tandem repeat6nstd128human GRCh37 (hg19) chr14: 75,907,822-75,907,862 , GRCh38 (hg38) chr14: 75,441,119-75,441,159 JDP2
    nsv1773027short tandem repeat5nstd128human GRCh37 (hg19) chr14: 75,900,251-75,900,267 , GRCh38 (hg38) chr14: 75,433,548-75,433,564 JDP2
    nsv1751981short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,914,659-75,914,678 , GRCh38 (hg38) chr14: 75,447,956-75,447,975 JDP2
    nsv1751980short tandem repeat4nstd128human GRCh37 (hg19) chr14: 75,910,613-75,910,623 , GRCh38 (hg38) chr14: 75,443,910-75,443,920 JDP2
    nsv1751979short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,897,470-75,897,501 , GRCh38 (hg38) chr14: 75,430,767-75,430,798 JDP2
    nsv1751623short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,936,189-75,936,221 , GRCh38 (hg38) chr14: 75,469,486-75,469,518 JDP2
    nsv1751622short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,906,725-75,906,744 , GRCh38 (hg38) chr14: 75,440,022-75,440,041 JDP2
    nsv1751621short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,897,514-75,897,527 , GRCh38 (hg38) chr14: 75,430,811-75,430,824 JDP2
    nsv1751520short tandem repeat7nstd128human GRCh37 (hg19) chr14: 75,936,876-75,936,892 , GRCh38 (hg38) chr14: 75,470,173-75,470,189 JDP2
    nsv1751519short tandem repeat1nstd128human GRCh37 (hg19) chr14: 75,914,366-75,914,380 , GRCh38 (hg38) chr14: 75,447,663-75,447,677 JDP2
    nsv1751518short tandem repeat2nstd128human GRCh37 (hg19) chr14: 75,894,991-75,895,020 , GRCh38 (hg38) chr14: 75,428,288-75,428,317 JDP2
    nsv1398265copy number variation1nstd102humanLikely pathogenic NCBI36 (hg18) chr14: 72,221,868-76,768,335 , GRCh38 (hg38) chr14: 72,685,407-77,232,239 , GRCh37 (hg19) chr14: 73,152,115-77,698,582 JDP2, ACYP1, 127 more genes
    nsv1195307copy number variation1nstd113human NCBI36 (hg18) chr14: 71,966,687-77,930,318 , GRCh37 (hg19) chr14: 72,896,934-78,860,565 , GRCh38 (hg38) chr14: 72,430,226-78,394,222 JDP2, PGF, 156 more genes
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