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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045068inversion1nstd229human GRCh38 chr4: 138,588,072-141,319,129 , GRCh37.p13 chr4: 139,509,226-142,240,283 RN7SKP253, FTH1P24, 41 more genes
    nsv7043921inversion1nstd229human GRCh38 chr4: 140,360,921-141,000,145 , GRCh37.p13 chr4: 141,282,075-141,921,299 UCP1, CLGN, 10 more genes
    nsv6755888copy number variation1nstd229human GRCh38 chr4: 140,462,225-140,465,129 , GRCh37.p13 chr4: 141,383,379-141,386,283 MGAT4D
    nsv6754613copy number variation1nstd229human GRCh38 chr4: 140,489,235-140,501,186 , GRCh37.p13 chr4: 141,410,389-141,422,340 MGAT4D
    nsv6753847copy number variation1nstd229human GRCh38 chr4: 140,484,401-140,498,800 , GRCh37.p13 chr4: 141,405,555-141,419,954 MGAT4D
    nsv6752742copy number variation1nstd229human GRCh38 chr4: 140,492,401-140,496,800 , GRCh37.p13 chr4: 141,413,555-141,417,954 MGAT4D
    nsv6751262copy number variation1nstd229human GRCh38 chr4: 140,479,934-140,487,870 , GRCh37.p13 chr4: 141,401,088-141,409,024 MGAT4D
    nsv6750559copy number variation1nstd229human GRCh38 chr4: 140,471,270-140,471,287 , GRCh37.p13 chr4: 141,392,424-141,392,441 MGAT4D
    nsv6750522copy number variation1nstd229human GRCh38 chr4: 140,449,767-140,460,634 , GRCh37.p13 chr4: 141,370,921-141,381,788 MGAT4D
    nsv6749380copy number variation1nstd229human GRCh38 chr4: 140,009,175-140,578,062 , GRCh37.p13 chr4: 140,930,329-141,499,216 SCOC-AS1, ELMOD2, 8 more genes
    nsv6748123copy number variation1nstd229human GRCh38 chr4: 140,437,899-140,440,385 , GRCh37.p13 chr4: 141,359,053-141,361,539 MGAT4D
    nsv6744473copy number variation1nstd229human GRCh38 chr4: 140,473,979-140,480,697 , GRCh37.p13 chr4: 141,395,133-141,401,851 MGAT4D
    nsv6743912copy number variation1nstd229human GRCh38 chr4: 140,226,102-140,524,180 , GRCh37.p13 chr4: 141,147,256-141,445,334 ELMOD2, CLGN, 4 more genes
    nsv6743197copy number variation1nstd229human GRCh38 chr4: 140,441,306-140,441,568 , GRCh37.p13 chr4: 141,362,460-141,362,722 MGAT4D
    nsv6739915copy number variation1nstd229human GRCh38 chr4: 140,468,382-140,475,129 , GRCh37.p13 chr4: 141,389,536-141,396,283 MGAT4D
    nsv6571624inversion1nstd223human GRCh38 chr4: 140,362,302-141,000,082 , GRCh37.p13 chr4: 141,283,456-141,921,236 RN7SL152P, UCP1, 10 more genes
    nsv6559786inversion1nstd223human GRCh38 chr4: 140,360,921-141,000,145 , GRCh37.p13 chr4: 141,282,075-141,921,299 TNRC18P1, RNY1P14, 10 more genes
    nsv6395137copy number variation1nstd223human GRCh38 chr4: 140,451,122-140,451,837 , GRCh37.p13 chr4: 141,372,276-141,372,991 MGAT4D
    nsv6395029copy number variation1nstd223human GRCh38 chr4: 140,450,823-140,451,195 , GRCh37.p13 chr4: 141,371,977-141,372,349 MGAT4D
    nsv6391492copy number variation1nstd223human GRCh38 chr4: 140,473,979-140,480,692 , GRCh37.p13 chr4: 141,395,133-141,401,846 MGAT4D
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