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Items: 1 to 20 of 397

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053235inversion1nstd229human GRCh38 chr7: 17,455,146-18,223,221 , GRCh37.p13 chr7: 17,494,770-18,262,844 SNX13, PRPS1L1, 6 more genes
    nsv7053118inversion1nstd229human GRCh38 chr7: 17,057,438-20,155,989 , GRCh37.p13 chr7: 17,097,062-20,195,612 MIR1302-6, LOC100419901, 29 more genes
    nsv7038576inversion1nstd229human GRCh38 chr7: 16,300,700-17,558,371 , GRCh37.p13 chr7: 16,340,325-17,597,995 LOC317727, LOC105375170, 21 more genes
    nsv6817820copy number variation1nstd229human GRCh38 chr7: 17,450,907-17,450,962 , GRCh37.p13 chr7: 17,490,531-17,490,586 LOC105375172, LINC02888
    nsv6814660copy number variation1nstd229human GRCh38 chr7: 17,386,479-17,515,486 , GRCh37.p13 chr7: 17,426,103-17,555,110 LINC02888, LOC105375172, 1 more genes
    nsv6814305copy number variation1nstd229human GRCh38 chr7: 17,363,707-17,447,401 , GRCh37.p13 chr7: 17,403,331-17,487,025 LOC105375171, LINC02888, 1 more genes
    nsv6814097copy number variation1nstd229human GRCh38 chr7: 16,798,427-17,711,088 , GRCh37.p13 chr7: 16,838,051-17,750,712 LOC100131425, LINC02888, 12 more genes
    nsv6813173copy number variation1nstd229human GRCh38 chr7: 17,385,803-17,691,727 , GRCh37.p13 chr7: 17,425,427-17,731,351 LINC02889, LINC02888, 1 more genes
    nsv6812617copy number variation1nstd229human GRCh38 chr7: 17,346,507-17,590,172 , GRCh37.p13 chr7: 17,386,131-17,629,796 LINC02889, LOC105375171, 3 more genes
    nsv6812189copy number variation1nstd229human GRCh38 chr7: 17,458,678-17,528,573 , GRCh37.p13 chr7: 17,498,302-17,568,197 LOC105375172, LINC02889, 1 more genes
    nsv6811078copy number variation1nstd229human GRCh38 chr7: 17,452,287-17,500,533 , GRCh37.p13 chr7: 17,491,911-17,540,157 LOC105375172, LINC02889, 1 more genes
    nsv6810863copy number variation1nstd229human GRCh38 chr7: 17,248,220-17,539,266 , GRCh37.p13 chr7: 17,287,844-17,578,890 AHR, LOC105375171, 4 more genes
    nsv6810634copy number variation1nstd229human GRCh38 chr7: 17,421,308-17,525,279 , GRCh37.p13 chr7: 17,460,932-17,564,903 LOC105375172, LINC02889, 1 more genes
    nsv6808371copy number variation1nstd229human GRCh38 chr7: 17,385,230-17,496,756 , GRCh37.p13 chr7: 17,424,854-17,536,380 LOC105375172, LINC02889, 1 more genes
    nsv6807706copy number variation1nstd229human GRCh38 chr7: 17,434,605-17,748,195 , GRCh37.p13 chr7: 17,474,229-17,787,819 LINC02888, LOC105375172, 1 more genes
    nsv6806580copy number variation1nstd229human GRCh38 chr7: 17,397,934-17,445,828 , GRCh37.p13 chr7: 17,437,558-17,485,452 LINC02888, LOC105375172
    nsv6805868copy number variation1nstd229human GRCh38 chr7: 17,388,955-17,547,119 , GRCh37.p13 chr7: 17,428,579-17,586,743 LINC02888, LOC105375172, 1 more genes
    nsv6805840copy number variation1nstd229human GRCh38 chr7: 17,383,543-17,524,282 , GRCh37.p13 chr7: 17,423,167-17,563,906 LOC105375172, LINC02889, 1 more genes
    nsv6805332copy number variation1nstd229human GRCh38 chr7: 17,388,739-17,438,420 , GRCh37.p13 chr7: 17,428,363-17,478,044 LOC105375172, LINC02888
    nsv6805135copy number variation1nstd229human GRCh38 chr7: 17,450,801-17,565,900 , GRCh37.p13 chr7: 17,490,425-17,605,524 LOC105375172, LINC02889, 1 more genes
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