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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
    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
    nsv6588406inversion1nstd223human GRCh38 chr16: 53,368,877-53,369,205 , GRCh37.p13 chr16: 53,402,789-53,403,117 MPHOSPH10P1
    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
    nsv6288608insertion1nstd214human GRCh38 chr16: 53,364,855-53,364,855 , GRCh37.p13 chr16: 53,398,767-53,398,767 MPHOSPH10P1
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 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
    nsv6092582insertion1nstd212human GRCh38 chr16: 53,364,858-53,364,858 , GRCh37.p13 chr16: 53,398,770-53,398,770 MPHOSPH10P1
    nsv5528427copy number variation1nstd206human GRCh38 chr16: 53,364,867-53,364,917 , GRCh37.p13 chr16: 53,398,779-53,398,829 MPHOSPH10P1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4709920copy number variation1nstd195human GRCh37 chr16: 53,384,451-53,431,451 , GRCh38.p12 chr16: 53,350,539-53,397,539 , MPHOSPH10P1, 2 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
    nsv4241156copy number variation1nstd166human GRCh37.p13 chr16: 53,398,779-53,398,829 , GRCh38.p12 chr16: 53,364,867-53,364,917 MPHOSPH10P1
    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
    nsv3920238copy number variation1nstd102humanUncertain significance GRCh37 chr16: 51,783,781-53,581,794 , GRCh38 chr16: 51,749,870-53,547,882 , NCBI36 chr16: 50,341,282-52,139,295 CASC16, LOC101929000, 30 more genes
    nsv3918594copy number variation1nstd102humanPathogenic GRCh38 chr16: 50,784,329-55,566,715 , NCBI36 chr16: 49,375,741-54,158,128 , GRCh37 chr16: 50,818,240-55,600,627 TOX3, CASC22, 74 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3917177copy number variation1nstd102humanPathogenic GRCh38 chr16: 49,570,553-53,467,065 , NCBI36 chr16: 48,161,965-52,058,478 , GRCh37 chr16: 49,604,464-53,500,977 LOC107984901, LOC100288763, 66 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
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