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Items: 1 to 20 of 326

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099204copy number variation1nstd231human GRCh38.p12 chr1: 51,433,462-53,162,521 , GRCh37 chr1: 51,899,134-53,628,193 EPS15, GPX7, 53 more genes
    nsv7052650inversion1nstd229human GRCh38 chr1: 47,584,744-54,395,558 , GRCh37.p13 chr1: 48,050,416-54,861,231 ANAPC10P1, SPATA6, 137 more genes
    nsv7043108inversion1nstd229human GRCh38 chr1: 52,460,709-52,460,832 , GRCh37.p13 chr1: 52,926,381-52,926,504 TUT4
    nsv6651646copy number variation1nstd229human GRCh38 chr1: 52,545,101-52,551,500 , GRCh37.p13 chr1: 53,010,773-53,017,172 TUT4, LOC105378723
    nsv6651644copy number variation1nstd229human GRCh38 chr1: 52,488,279-52,488,373 , GRCh37.p13 chr1: 52,953,951-52,954,045 TUT4
    nsv6651560copy number variation1nstd229human GRCh38 chr1: 52,426,260-52,461,707 , GRCh37.p13 chr1: 52,891,932-52,927,379 TUT4
    nsv6651428copy number variation1nstd229human GRCh38 chr1: 52,553,490-52,561,309 , GRCh37.p13 chr1: 53,019,162-53,026,981 TUT4
    nsv6651427copy number variation1nstd229human GRCh38 chr1: 52,533,557-52,534,012 , GRCh37.p13 chr1: 52,999,229-52,999,684 TUT4, LOC105378723
    nsv6651426copy number variation1nstd229human GRCh38 chr1: 52,494,244-52,494,744 , GRCh37.p13 chr1: 52,959,916-52,960,416 TUT4
    nsv6651425copy number variation1nstd229human GRCh38 chr1: 52,485,147-52,485,772 , GRCh37.p13 chr1: 52,950,819-52,951,444 TUT4
    nsv6650896copy number variation1nstd229human GRCh38 chr1: 52,541,971-52,542,055 , GRCh37.p13 chr1: 53,007,643-53,007,727 TUT4, LOC105378723
    nsv6650895copy number variation1nstd229human GRCh38 chr1: 52,514,257-52,514,435 , GRCh37.p13 chr1: 52,979,929-52,980,107 TUT4
    nsv6650894copy number variation1nstd229human GRCh38 chr1: 52,455,934-52,457,673 , GRCh37.p13 chr1: 52,921,606-52,923,345 TUT4
    nsv6650893copy number variation1nstd229human GRCh38 chr1: 52,422,360-52,422,394 , GRCh37.p13 chr1: 52,888,032-52,888,066 TUT4
    nsv6638064copy number variation1nstd102humanassociation GRCh38 chr1: 48,666,286-52,808,894 , GRCh37.p13 chr1: 49,131,958-53,274,566 LOC105378710, RNU6-1026P, 80 more genes
    nsv6555337inversion1nstd223human GRCh38 chr1: 52,456,180-52,457,370 , GRCh37.p13 chr1: 52,921,852-52,923,042 TUT4
    nsv6551426inversion1nstd223human GRCh38 chr1: 52,523,027-52,523,581 , GRCh37.p13 chr1: 52,988,699-52,989,253 TUT4
    nsv6547733inversion1nstd223human GRCh38 chr1: 52,521,114-52,521,286 , GRCh37.p13 chr1: 52,986,786-52,986,958 TUT4
    nsv6544144inversion1nstd223human GRCh38 chr1: 52,543,488-52,544,273 , GRCh37.p13 chr1: 53,009,160-53,009,945 LOC105378723, TUT4
    nsv6543789inversion1nstd223human GRCh38 chr1: 52,521,005-52,521,758 , GRCh37.p13 chr1: 52,986,677-52,987,430 TUT4
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