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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5462593copy number variation1nstd206human GRCh38 chr6: 159,522,508-159,529,507 , GRCh37.p13 chr6: 159,943,540-159,950,539 RPL21P69
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 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
    nsv4410531copy number variation1nstd174human GRCh37 chr6: 159,509,373-160,043,247 , GRCh38.p12 chr6: 159,088,341-159,622,215 FNDC1, RPL21P69, 6 more genes
    nsv4378261copy number variation1nstd173human GRCh37 chr6: 159,929,460-159,986,505 , GRCh38.p12 chr6: 159,508,428-159,565,473 RPL21P69
    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
    nsv3921491copy number variation1nstd102humanPathogenic NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089 LOC102724357, LOC101929142, 183 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
    nsv3913213copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240 LDHAL6FP, QKI, 258 more genes
    nsv3913037copy number variation1nstd102humanPathogenic GRCh37 chr6: 152,697,473-170,921,089 , GRCh38 chr6: 152,376,338-170,612,001 , NCBI36 chr6: 152,739,166-170,763,014 KRT8P44, TULP4, 283 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
    nsv3911475copy number variation1nstd102humanPathogenic GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407 SNORA116, PRR18, 275 more genes
    nsv3909469copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,155,998-171,054,786 , GRCh38.p12 chr6: 158,734,966-170,745,698 LOC101929614, FNDC1, 203 more genes
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