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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7055434inversion1nstd229human GRCh38 chr5: 139,679,545-139,690,742 , GRCh37.p13 chr5: 139,059,130-139,070,327 CXXC5
    nsv7054464inversion1nstd229human GRCh38 chr5: 139,677,062-139,680,868 , GRCh37.p13 chr5: 139,056,647-139,060,453 CXXC5
    nsv7049767inversion1nstd229human GRCh38 chr5: 139,676,602-139,676,660 , GRCh37.p13 chr5: 139,056,187-139,056,245 CXXC5
    nsv7044263inversion1nstd229human GRCh38 chr5: 139,680,865-139,690,743 , GRCh37.p13 chr5: 139,060,450-139,070,328 CXXC5
    nsv6796083copy number variation1nstd229human GRCh38 chr5: 139,656,542-139,657,333 , GRCh37.p13 chr5: 139,036,127-139,036,918 CXXC5
    nsv6794480copy number variation1nstd229human GRCh38 chr5: 139,683,365-139,689,454 , GRCh37.p13 chr5: 139,062,950-139,069,039 CXXC5
    nsv6793506copy number variation1nstd229human GRCh38 chr5: 139,668,823-139,671,180 , GRCh37.p13 chr5: 139,048,408-139,050,765 CXXC5
    nsv6790080copy number variation1nstd229human GRCh38 chr5: 139,512,801-139,911,500 , GRCh37.p13 chr5: 138,892,386-139,291,085 PSD2, HSPE1P15, 7 more genes
    nsv6781978copy number variation1nstd229human GRCh38 chr5: 139,680,801-139,691,000 , GRCh37.p13 chr5: 139,060,386-139,070,585 CXXC5
    nsv6778497copy number variation1nstd229human GRCh38 chr5: 139,616,130-139,666,617 , GRCh37.p13 chr5: 138,995,715-139,046,202 CXXC5, UBE2D2, 1 more genes
    nsv6413204copy number variation1nstd223human GRCh38 chr5: 139,677,533-139,680,308 , GRCh37.p13 chr5: 139,057,118-139,059,893 CXXC5
    nsv6406690copy number variation1nstd223human GRCh38 chr5: 139,671,626-139,674,711 , GRCh37.p13 chr5: 139,051,211-139,054,296 CXXC5
    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
    nsv6400624copy number variation1nstd223human GRCh38 chr5: 139,668,001-139,668,600 , GRCh37.p13 chr5: 139,047,586-139,048,185 CXXC5
    nsv6397691copy number variation1nstd223human GRCh38 chr5: 139,668,823-139,671,175 , GRCh37.p13 chr5: 139,048,408-139,050,760 CXXC5
    nsv6397544copy number variation1nstd223human GRCh38 chr5: 139,683,376-139,690,579 , GRCh37.p13 chr5: 139,062,961-139,070,164 CXXC5
    nsv6300027copy number variation1nstd186human GRCh37 chr5: 139,049,103-139,049,361 , GRCh38.p12 chr5: 139,669,518-139,669,776 CXXC5
    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
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