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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094848copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,635,988-54,967,785 , GRCh38.p12 chr16: 53,602,076-54,933,873 LOC105371271, LOC105371272, 13 more genes
    nsv7094675copy number variation1nstd102humanPathogenic GRCh37 chr16: 53,635,988-55,539,614 , GRCh38.p12 chr16: 53,602,076-55,505,702 LOC105371276, LINC02183, 22 more genes
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv6993586copy number variation1nstd229human GRCh38 chr16: 54,817,161-54,930,763 , GRCh37.p13 chr16: 54,851,073-54,964,675 LOC105371275, LOC105371276, 3 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623676copy number variation1nstd224human GRCh37 chr16: 54,948,857-55,088,225 , GRCh38.p12 chr16: 54,914,945-55,054,313 IRX5, CRNDE, 3 more genes
    nsv6587757inversion1nstd223human GRCh38 chr16: 54,916,617-54,916,977 , GRCh37.p13 chr16: 54,950,529-54,950,889 CRNDE
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6289807copy number variation1nstd102humanPathogenic GRCh38 chr16: 54,801,236-55,533,834 , GRCh37.p13 chr16: 54,835,148-55,567,746 LOC105371278, LOC105371275, 13 more genes
    nsv6289796copy number variation1nstd102humanPathogenic GRCh38 chr16: 54,893,325-55,501,091 , GRCh37.p13 chr16: 54,927,237-55,535,003 MMP2, CRNDE, 10 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6132994copy number variation1nstd213human GRCh37 chr16: 54,920,000-54,980,001 , GRCh38.p12 chr16: 54,886,088-54,946,089 IRX5, CRNDE, 1 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 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
    nsv4498585mobile element insertion1nstd166human GRCh37.p13 chr16: 54,956,313-54,956,313 , GRCh38.p12 chr16: 54,922,401-54,922,401 CRNDE
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
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