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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2777872copy number variation4nstd37humanPathogenic GRCh37 (hg19) chr18: 163,323-78,005,185 , GRCh38 (hg38) chr18: 163,323-80,247,302 , NCBI36 (hg18) chr18: 153,323-76,106,176 CDH2, ZSCAN30, 379 more genes
    nsv2776693copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr18: 20,069,932-36,887,326 , GRCh38 (hg38) chr18: 22,489,969-39,307,362 , NCBI36 (hg18) chr18: 18,323,930-35,141,324 CDH2, ZSCAN30, 74 more genes
    nsv2776649copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr18: 15,370,696-76,117,153 , GRCh37 (hg19) chr18: 15,380,696-78,016,181 , GRCh38 (hg38) chr18: 15,380,697-80,258,298 CDH2, ZSCAN30, 277 more genes
    nsv2776640copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr18: 24,835,114-46,917,217 , GRCh38 (hg38) chr18: 27,255,150-49,390,847 , NCBI36 (hg18) chr18: 23,089,112-45,171,215 CDH2, ZSCAN30, 92 more genes
    nsv2773275copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr18: 136,227-46,171,053 , GRCh38 (hg38) chr18: 136,227-48,644,682 , NCBI36 (hg18) chr18: 126,227-44,425,051 CDH2, ZSCAN30, 232 more genes
    nsv2770755copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr18: 18,521,285-64,495,798 , GRCh38 (hg38) chr18: 20,941,324-66,828,561 , NCBI36 (hg18) chr18: 16,775,283-62,646,778 CDH2, ZSCAN30, 227 more genes
    esv3881325copy number variation1estd219human GRCh37 (hg19) chr18: 29,106,287-29,106,394 , GRCh38 (hg38) chr18: 31,526,324-31,526,431 DSG2
    nsv1909057short tandem repeat5nstd128human GRCh37 (hg19) chr18: 29,122,923-29,122,943 , GRCh38 (hg38) chr18: 31,542,960-31,542,980 DSG2-AS1, DSG2
    nsv1909056short tandem repeat1nstd128human GRCh37 (hg19) chr18: 29,110,685-29,110,698 , GRCh38 (hg38) chr18: 31,530,722-31,530,735 DSG2
    nsv1909055short tandem repeat1nstd128human GRCh37 (hg19) chr18: 29,109,284-29,109,302 , GRCh38 (hg38) chr18: 31,529,321-31,529,339 DSG2
    nsv1909054short tandem repeat2nstd128human GRCh37 (hg19) chr18: 29,098,689-29,098,699 , GRCh38 (hg38) chr18: 31,518,726-31,518,736 DSG2
    nsv1907865short tandem repeat3nstd128human GRCh37 (hg19) chr18: 29,127,640-29,127,666 , GRCh38 (hg38) chr18: 31,547,677-31,547,703 DSG2-AS1, DSG2
    nsv1907864short tandem repeat1nstd128human GRCh37 (hg19) chr18: 29,125,253-29,125,268 , GRCh38 (hg38) chr18: 31,545,290-31,545,305 DSG2-AS1, DSG2
    nsv1907862short tandem repeat3nstd128human GRCh37 (hg19) chr18: 29,115,733-29,115,756 , GRCh38 (hg38) chr18: 31,535,770-31,535,793 DSG2
    nsv1907861short tandem repeat8nstd128human GRCh37 (hg19) chr18: 29,113,946-29,113,971 , GRCh38 (hg38) chr18: 31,533,983-31,534,008 DSG2
    nsv1907860short tandem repeat8nstd128human GRCh37 (hg19) chr18: 29,112,871-29,112,901 , GRCh38 (hg38) chr18: 31,532,908-31,532,938 DSG2
    nsv1907859short tandem repeat4nstd128human GRCh37 (hg19) chr18: 29,101,216-29,101,230 , GRCh38 (hg38) chr18: 31,521,253-31,521,267 DSG2
    nsv1907858short tandem repeat3nstd128human GRCh37 (hg19) chr18: 29,090,554-29,090,566 , GRCh38 (hg38) chr18: 31,510,591-31,510,603 DSG2
    nsv1907857short tandem repeat3nstd128human GRCh37 (hg19) chr18: 29,082,720-29,082,782 , GRCh38 (hg38) chr18: 31,502,757-31,502,819 DSG2
    nsv1907628short tandem repeat2nstd128human GRCh37 (hg19) chr18: 29,117,964-29,117,981 , GRCh38 (hg38) chr18: 31,538,001-31,538,018 DSG2
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