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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057334inversion1nstd229human GRCh38 chr3: 44,364,383-44,373,794 , GRCh37.p13 chr3: 44,405,875-44,415,286 TCAIM
    nsv7051996inversion1nstd229human GRCh38 chr3: 43,186,996-45,060,828 , GRCh37.p13 chr3: 43,228,488-45,102,320 ABHD5, CLEC3B, 44 more genes
    nsv7043252inversion1nstd229human GRCh38 chr3: 44,403,523-44,403,596 , GRCh37.p13 chr3: 44,445,015-44,445,088 TCAIM
    nsv7038909inversion1nstd229human GRCh38 chr3: 40,520,096-45,093,302 , GRCh37.p13 chr3: 40,561,587-45,134,794 ABHD5, ZKSCAN7, 97 more genes
    nsv6718001copy number variation1nstd229human GRCh38 chr3: 44,393,518-44,393,912 , GRCh37.p13 chr3: 44,435,010-44,435,404 TCAIM
    nsv6715107copy number variation1nstd229human GRCh38 chr3: 44,373,121-44,373,146 , GRCh37.p13 chr3: 44,414,613-44,414,638 TCAIM
    nsv6713116copy number variation1nstd229human GRCh38 chr3: 44,340,603-44,345,339 , GRCh37.p13 chr3: 44,382,095-44,386,831 TCAIM
    nsv6711076copy number variation1nstd229human GRCh38 chr3: 44,340,475-44,340,703 , GRCh37.p13 chr3: 44,381,967-44,382,195 TCAIM
    nsv6707084copy number variation1nstd229human GRCh38 chr3: 44,378,897-44,385,507 , GRCh37.p13 chr3: 44,420,389-44,426,999 TCAIM
    nsv6706862copy number variation1nstd229human GRCh38 chr3: 43,255,168-44,930,739 , GRCh37.p13 chr3: 43,296,660-44,972,231 LOC101928529, ANO10, 40 more genes
    nsv6701336copy number variation1nstd229human GRCh38 chr3: 44,344,511-44,352,329 , GRCh37.p13 chr3: 44,386,003-44,393,821 TCAIM
    nsv6700725copy number variation1nstd229human GRCh38 chr3: 44,399,241-44,399,304 , GRCh37.p13 chr3: 44,440,733-44,440,796 TCAIM
    nsv6546796inversion1nstd223human GRCh38 chr3: 44,343,054-44,344,273 , GRCh37.p13 chr3: 44,384,546-44,385,765 TCAIM
    nsv6543496inversion1nstd223human GRCh38 chr3: 44,372,615-44,373,527 , GRCh37.p13 chr3: 44,414,107-44,415,019 TCAIM
    nsv6536783inversion1nstd223human GRCh38 chr3: 44,370,468-44,371,105 , GRCh37.p13 chr3: 44,411,960-44,412,597 TCAIM
    nsv6374057copy number variation1nstd223human GRCh38 chr3: 44,335,401-44,340,500 , GRCh37.p13 chr3: 44,376,893-44,381,992 TCAIM, TOPAZ1, 1 more genes
    nsv6372831copy number variation1nstd223human GRCh38 chr3: 44,340,603-44,345,351 , GRCh37.p13 chr3: 44,382,095-44,386,843 TCAIM
    nsv6372608copy number variation1nstd223human GRCh38 chr3: 44,345,670-44,348,897 , GRCh37.p13 chr3: 44,387,162-44,390,389 TCAIM
    nsv6366759copy number variation1nstd223human GRCh38 chr3: 44,401,582-44,402,034 , GRCh37.p13 chr3: 44,443,074-44,443,526 TCAIM
    nsv6363859copy number variation1nstd223human GRCh38 chr3: 44,378,897-44,385,480 , GRCh37.p13 chr3: 44,420,389-44,426,972 TCAIM
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