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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051940inversion1nstd229human GRCh38 chr6: 28,627,967-29,067,478 , GRCh37.p13 chr6: 28,595,744-29,035,255 ZNF90P2, TRK-TTT13-1, 51 more genes
    nsv6792440copy number variation1nstd229human GRCh38 chr6: 28,727,674-28,790,107 , GRCh37.p13 chr6|NT_167248.1: 1-61,285 , GRCh37.p13 chr6|NT_167246.1: 1-61,285 , GRCh37.p13 chr6: 28,695,451-28,757,884 TRF-GAA1-1, TRK-TTT7-1, 8 more genes
    nsv6778116copy number variation1nstd229human GRCh38 chr6: 28,725,457-28,820,877 , GRCh37.p13 chr6|NT_167248.1: 1-92,055 , GRCh37.p13 chr6|NT_167246.1: 1-92,055 , GRCh37.p13 chr6: 28,693,234-28,788,654 TRA-TGC6-1, TRA-CGC4-1, 13 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6395626copy number variation1nstd223human GRCh38 chr6: 28,725,457-28,820,877 , GRCh37.p13 chr6: 28,693,234-28,788,654 , GRCh37.p13 chr6|NT_167246.1: 1-92,055 , GRCh37.p13 chr6|NT_167248.1: 1-92,055 TRA-TGC6-1, TRA-CGC4-1, 13 more genes
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6135508copy number variation1nstd213human GRCh37 chr6: 27,710,000-30,110,001 , GRCh38.p12 chr6: 27,742,221-30,142,224 GABBR1, H1-5, 224 more genes
    nsv5471232copy number variation1nstd206human GRCh38 chr6: 28,557,707-28,888,244 , GRCh37.p13 chr6: 28,525,484-28,856,021 TRA-TGC5-1, TRA-AGC1-1, 33 more genes
    nsv5197442mobile element insertion1nstd203human GRCh38 chr6: 28,790,282-28,790,298 , GRCh37.p13 chr6|NT_167248.1: 61,460-61,476 , GRCh37.p13 chr6|NT_167246.1: 61,460-61,476 , GRCh37.p13 chr6: 28,758,059-28,758,075 TRA-TGC1-1, TRF-GAA1-1
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4397091copy number variation1nstd174human GRCh37 chr6: 28,758,645-28,780,578 , GRCh38.p12 chr6: 28,790,868-28,812,801 TRF-GAA1-1, TRA-AGC1-1, 1 more genes
    nsv4369356copy number variation2nstd173human GRCh37 chr6: 28,756,483-28,779,637 , GRCh38.p12 chr6: 28,788,706-28,811,860 TRF-GAA3-1, TRF-GAA1-1, 2 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3916231copy number variation1nstd102humanBenign GRCh38 chr6: 28,669,195-28,873,863 , GRCh37 chr6: 28,636,972-28,841,640 , NCBI36 chr6: 28,744,951-28,949,619 TRA-TGC6-1, TRK-TTT7-1, 21 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3912336copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,730,964-29,737,605 , GRCh38 chr6: 28,763,187-29,769,828 , NCBI36 chr6: 28,838,943-29,845,584 OR2AD1P, UBD, 87 more genes
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