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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5466968copy number variation1nstd206human GRCh38 chr6: 159,044,120-159,044,198 , GRCh37.p13 chr6: 159,465,152-159,465,230 , TAGAP, 1 more genes
    nsv5239492copy number variation1nstd204human GRCh38.p13 chr6: 159,036,567-159,039,689 , GRCh37.p13 chr6: 159,457,599-159,460,721 TAGAP-AS1, TAGAP
    nsv5220972copy number variation1nstd204human GRCh38.p13 chr6: 159,040,690-159,043,089 , GRCh37.p13 chr6: 159,461,722-159,464,121 TAGAP-AS1, TAGAP
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4680332copy number variation1nstd189human GRCh37.p13 chr6: 159,378,922-159,581,236 , GRCh38.p12 chr6: 158,957,890-159,160,204 , RSPH3, 3 more genes
    nsv4618454copy number variation1nstd183human GRCh37 chr6: 159,407,526-159,535,533 , GRCh38.p12 chr6: 158,986,494-159,114,501 , TAGAP, 3 more genes
    nsv4611515copy number variation1nstd183human GRCh37 chr6: 159,459,099-159,461,305 , GRCh38.p12 chr6: 159,038,067-159,040,273 TAGAP-AS1, TAGAP
    nsv4606028copy number variation1nstd183human GRCh37 chr6: 159,461,955-159,464,934 , GRCh38.p12 chr6: 159,040,923-159,043,902 , TAGAP-AS1, 1 more genes
    nsv4599357copy number variation1nstd183human GRCh37 chr6: 159,456,391-159,466,279 , GRCh38.p12 chr6: 159,035,359-159,045,247 , TAGAP, 1 more genes
    nsv4497036mobile element insertion1nstd166human GRCh37.p13 chr6: 159,464,992-159,464,992 , GRCh38.p12 chr6: 159,043,960-159,043,960 , TAGAP, 1 more genes
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4455446copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,262,571-160,992,289 , GRCh38.p12 chr6: 156,941,437-160,571,257 LOC105378076, LOC107986663, 67 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3921695copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595 LOC105378128, LOC105378102, 255 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
    nsv3918864copy number variation1nstd102humanPathogenic GRCh38 chr6: 157,827,805-159,726,548 , NCBI36 chr6: 158,168,825-160,067,570 , GRCh37 chr6: 158,248,837-160,147,580 GTF2H5, SNORA116, 39 more genes
    nsv3916405copy number variation1nstd102humanPathogenic NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984 LOC112267968, ARMT1, 126 more genes
    nsv3916251copy number variation1nstd102humanPathogenic GRCh38 chr6: 155,378,049-163,133,499 , NCBI36 chr6: 155,740,875-163,474,521 , GRCh37 chr6: 155,699,183-163,554,531 MAP3K4, LOC112267977, 99 more genes
    nsv3915573copy number variation1nstd102humanUncertain significance NCBI36 chr6: 158,926,744-161,240,805 , GRCh37 chr6: 159,006,756-161,320,815 , GRCh38 chr6: 158,585,724-160,899,783 TAGAP-AS1, PNLDC1, 48 more genes
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