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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5597988copy number variation1nstd207human GRCh38 chr16: 31,567,791-31,569,797 , GRCh37.p13 chr16: 31,579,112-31,581,118 FRG2KP, YBX3P1
    nsv5524212copy number variation1nstd206human GRCh38 chr16: 31,562,486-31,596,486 , GRCh37.p13 chr16: 31,573,807-31,607,807 YBX3P1, FRG2KP
    nsv5518595copy number variation1nstd206human GRCh38 chr16: 31,553,145-31,626,891 , GRCh37.p13 chr16: 31,564,466-31,638,212 LINC02190, YBX3P1, 3 more genes
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv5003538copy number variation1nstd200human GRCh38 chr16: 31,553,087-31,572,430 , GRCh37.p13 chr16: 31,564,408-31,583,751 YBX3P1, LINC02190, 2 more genes
    nsv4994629copy number variation1nstd200human GRCh38 chr16: 31,553,112-31,626,891 , GRCh37.p13 chr16: 31,564,433-31,638,212 YBX3P1, KRBOX5P1, 3 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4504101mobile element insertion1nstd166human GRCh37.p13 chr16: 31,578,588-31,578,588 , GRCh38.p12 chr16: 31,567,267-31,567,267 FRG2KP, YBX3P1
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4420411copy number variation1nstd174human GRCh37 chr16: 31,526,789-31,822,853 , GRCh38.p12 chr16: 31,515,468-31,811,532 , LINC02190, 14 more genes
    nsv4383368copy number variation1nstd173human GRCh37 chr16: 31,567,485-31,630,503 , GRCh38.p12 chr16: 31,556,164-31,619,182 FRG2KP, KRBOX5P1, 1 more genes
    nsv4368667copy number variation1nstd173human GRCh37 chr16: 31,572,397-31,633,179 , GRCh38.p12 chr16: 31,561,076-31,621,858 KRBOX5P1, YBX3P1, 1 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4252299copy number variation1nstd166human GRCh37.p13 chr16: 31,564,433-31,638,212 , GRCh38.p12 chr16: 31,553,112-31,626,891 LINC02190, KRBOX5P1, 3 more genes
    nsv3959679copy number variation1nstd168human GRCh38 chr16: 31,510,785-31,566,618 , GRCh37.p13 chr16: 31,522,106-31,577,939 AHSP, YBX3P1, 4 more genes
    nsv3918492copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,703,233-35,147,508 , NCBI36 chr16: 30,610,734-35,005,009 , GRCh38 chr16: 30,691,912-36,160,463 KRBOX5P1, LOC110262331, 213 more genes
    nsv3914248copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577 ZG16, TPRKBP2, 250 more genes
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