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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097024copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,266,142-138,861,289 , GRCh38.p12 chr5: 138,930,453-139,481,704 SLC23A1, RNU5B-4P, 20 more genes
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6795812copy number variation1nstd229human GRCh38 chr5: 139,429,733-139,435,791 , GRCh37.p13 chr5: 138,765,422-138,771,480 DNAJC18
    nsv6794526copy number variation1nstd229human GRCh38 chr5: 139,400,923-139,411,448 , GRCh37.p13 chr5: 138,736,612-138,747,137 DNAJC18, SPATA24
    nsv6786593copy number variation1nstd229human GRCh38 chr5: 139,425,944-139,433,006 , GRCh37.p13 chr5: 138,761,633-138,768,695 DNAJC18
    nsv6636861copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,893,096-138,868,605 , GRCh38.p12 chr5: 138,557,407-139,489,020 HSPA9, ECSCR, 27 more genes
    nsv6630305copy number variation1nstd224human GRCh37 chr5: 138,652,744-138,764,329 , GRCh38.p12 chr5: 139,317,055-139,428,640 MATR3, SLC23A1, 6 more genes
    nsv6575066inversion1nstd223human GRCh38 chr5: 139,416,945-139,417,699 , GRCh37.p13 chr5: 138,752,634-138,753,388 DNAJC18
    nsv6565385inversion1nstd223human GRCh38 chr5: 139,417,002-139,417,758 , GRCh37.p13 chr5: 138,752,691-138,753,447 DNAJC18
    nsv6410153copy number variation1nstd223human GRCh38 chr5: 139,418,371-139,425,393 , GRCh37.p13 chr5: 138,754,060-138,761,082 DNAJC18
    nsv6407453copy number variation1nstd223human GRCh38 chr5: 139,415,962-139,418,811 , GRCh37.p13 chr5: 138,751,651-138,754,500 DNAJC18
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6399113copy number variation1nstd223human GRCh38 chr5: 139,400,918-139,411,449 , GRCh37.p13 chr5: 138,736,607-138,747,138 DNAJC18, SPATA24
    nsv6291250copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,386,858-138,935,115 , GRCh38.p12 chr5: 139,051,169-139,555,530 STING1, SPATA24, 18 more genes
    nsv6291016copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,675,227-139,314,012 , GRCh38.p12 chr5: 139,339,538-139,934,427 PROB1, H3P25, 19 more genes
    nsv6135654copy number variation1nstd213human GRCh37 chr5: 138,770,000-138,890,001 , GRCh38.p12 chr5: 139,434,311-139,510,416 DNAJC18, STING1, 5 more genes
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
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