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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3053753insertion1nstd140human GRCh38 (hg38) chr16: 46,675,093-46,675,094 , GRCh37 (hg19) chr16: 46,709,005-46,709,006 VPS35
    nsv2779201copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37 (hg19) chr16: 31,986,098-90,294,753 , GRCh38 (hg38) chr16: 31,974,777-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2778249copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr16: 69,193-90,274,381 , GRCh38 (hg38) chr16: 19,193-90,207,973 , NCBI36 (hg18) chr16: 9,193-88,801,882 CDH3, SNORD111B, 1093 more genes
    nsv2777803copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr16: 46,503,406-46,842,785 , GRCh38 (hg38) chr16: 46,469,494-46,808,873 , NCBI36 (hg18) chr16: 45,060,907-45,400,286 ORC6, C16orf87, 3 more genes
    nsv2777058copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 32,348,376-88,822,254 , GRCh37 (hg19) chr16: 32,440,875-90,294,753 , GRCh38 (hg38) chr16: 32,429,554-90,228,345 CDH3, SNORD111B, 513 more genes
    nsv2777039copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr16: 9,273,328-89,548,493 , GRCh38 (hg38) chr16: 9,179,471-89,482,085 , NCBI36 (hg18) chr16: 9,180,829-88,075,994 CDH3, SNORD111B, 808 more genes
    nsv2777010copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr16: 85,881-90,155,062 , GRCh38 (hg38) chr16: 35,881-90,088,654 , NCBI36 (hg18) chr16: 25,881-88,682,563 CDH3, SNORD111B, 1089 more genes
    nsv2776654copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr16: 46,464,488-90,155,062 , GRCh38 (hg38) chr16: 46,430,576-90,088,654 , NCBI36 (hg18) chr16: 45,021,989-88,682,563 CDH3, SNORD111B, 477 more genes
    nsv2775655copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37 (hg19) chr16: 31,986,098-90,294,753 , GRCh38 (hg38) chr16: 31,974,777-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2775454copy number variation2nstd37humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37 (hg19) chr16: 31,986,098-90,294,753 , GRCh38 (hg38) chr16: 31,974,777-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2774817copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr16: 46,509,686-46,843,488 , GRCh38 (hg38) chr16: 46,475,774-46,809,576 , NCBI36 (hg18) chr16: 45,067,187-45,400,989 ORC6, C16orf87, 3 more genes
    nsv2774561copy number variation2nstd37humanBenign NCBI36 (hg18) chr16: 32,481,314-88,822,254 , GRCh37 (hg19) chr16: 32,573,813-90,294,753 , GRCh38 (hg38) chr16: 32,562,492-90,228,345 CDH3, SNORD111B, 513 more genes
    nsv2772976copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 31,862,658-88,822,254 , GRCh37 (hg19) chr16: 31,955,157-90,294,753 , GRCh38 (hg38) chr16: 31,943,836-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2772305copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 32,529,496-88,822,254 , GRCh37 (hg19) chr16: 32,621,995-90,294,753 , GRCh38 (hg38) chr16: 32,610,674-90,228,345 CDH3, SNORD111B, 513 more genes
    nsv2771961copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 31,902,168-88,822,254 , GRCh37 (hg19) chr16: 31,994,667-90,294,753 , GRCh38 (hg38) chr16: 31,983,346-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2769774copy number variation1nstd37humanBenign NCBI36 (hg18) chr16: 31,902,168-88,822,254 , GRCh37 (hg19) chr16: 31,994,667-90,294,753 , GRCh38 (hg38) chr16: 31,983,346-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2768706copy number variation2nstd37humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37 (hg19) chr16: 31,986,098-90,294,753 , GRCh38 (hg38) chr16: 31,974,777-90,228,345 CDH3, SNORD111B, 515 more genes
    nsv2768704copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr16: 35,006,660-45,286,576 , GRCh37 (hg19) chr16: 35,149,159-46,729,075 , GRCh38 (hg38) chr16: 35,914,788-46,695,163 ORC6, VPS35, 1 more genes
    esv3877379copy number variation1estd219human GRCh37 (hg19) chr16: 46,581,009-46,749,921 , GRCh38 (hg38) chr16: 46,547,097-46,716,009 ORC6, VPS35, 2 more genes
    esv3877386copy number variation1estd219human GRCh37 (hg19) chr16: 46,711,913-46,772,692 , GRCh38 (hg38) chr16: 46,678,001-46,738,780 ORC6, VPS35, 1 more genes
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