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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7069168inversion1nstd229human GRCh38 chr15: 65,085,774-67,006,275 , GRCh37.p13 chr15: 65,378,112-67,298,613 MEGF11, HNRNPA1P44, 51 more genes
    nsv6967827copy number variation1nstd229human GRCh38 chr15: 66,386,041-66,735,404 , GRCh37.p13 chr15: 66,678,379-67,027,742 ATP5MFP6, SMAD6, 13 more genes
    nsv6964058copy number variation1nstd229human GRCh38 chr15: 66,547,104-66,575,404 , GRCh37.p13 chr15: 66,839,442-66,867,742 LCTL, ZWILCH
    nsv6962751copy number variation1nstd229human GRCh38 chr15: 66,533,237-66,546,401 , GRCh37.p13 chr15: 66,825,575-66,838,739 LCTL, ZWILCH
    nsv6595235inversion1nstd223human GRCh38 chr15: 66,562,122-66,562,807 , GRCh37.p13 chr15: 66,854,460-66,855,145 LCTL
    nsv6514258copy number variation1nstd223human GRCh38 chr15: 66,551,317-66,553,843 , GRCh37.p13 chr15: 66,843,655-66,846,181 LCTL
    nsv6504894copy number variation1nstd223human GRCh38 chr15: 66,554,143-66,555,372 , GRCh37.p13 chr15: 66,846,481-66,847,710 LCTL
    nsv6497578copy number variation1nstd223human GRCh38 chr15: 66,533,237-66,546,400 , GRCh37.p13 chr15: 66,825,575-66,838,738 LCTL, ZWILCH
    nsv6309802copy number variation2nstd102humanUncertain significance GRCh37 chr15: 66,161,924-69,018,313 , GRCh38.p12 chr15: 65,869,586-68,725,974 SNORD18B, TRQ-CTG1-4, 50 more genes
    nsv6133153copy number variation1nstd213human GRCh37 chr15: 66,740,000-66,910,001 , GRCh38.p12 chr15: 66,447,662-66,617,663 MAP2K1, RPL4, 9 more genes
    nsv6024287copy number variation1nstd212human GRCh38 chr15: 66,559,898-66,562,199 , GRCh37.p13 chr15: 66,852,236-66,854,537 LCTL
    nsv5527227copy number variation1nstd206human GRCh38 chr15: 66,553,572-66,554,141 , GRCh37.p13 chr15: 66,845,910-66,846,479 LCTL
    nsv5515055copy number variation1nstd206human GRCh38 chr15: 66,551,132-66,554,009 , GRCh37.p13 chr15: 66,843,470-66,846,347 LCTL
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5344852translocation1nstd200human GRCh37 chr1: 25,955,634-25,955,634 , GRCh37 chr15: 66,841,266-66,841,266 , GRCh38.p12 chr1: 25,629,143-25,629,143 , GRCh38.p12 chr15: 66,548,928-66,548,928 ZWILCH, MAN1C1, 1 more genes
    nsv5143410mobile element insertion1nstd203human GRCh38 chr15: 66,559,922-66,559,958 , GRCh37.p13 chr15: 66,852,260-66,852,296 LCTL
    nsv4992091copy number variation1nstd200human GRCh38 chr15: 66,565,415-66,570,148 , GRCh37.p13 chr15: 66,857,753-66,862,486 LCTL
    nsv4350627copy number variation1nstd102humanPathogenic GRCh37 chr15: 66,817,545-67,418,205 , GRCh38.p12 chr15: 66,525,207-67,125,867 LETM1P1, SMAD6, 9 more genes
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