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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071647inversion1nstd229human GRCh38 chr15: 54,705,615-56,525,786 , GRCh37.p13 chr15: 54,997,813-56,817,984 RN7SL568P, CD24P2, 21 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv6967323copy number variation1nstd229human GRCh38 chr15: 56,389,498-56,457,109 , GRCh37.p13 chr15: 56,681,696-56,749,307 MNS1, TEX9
    nsv6965989copy number variation1nstd229human GRCh38 chr15: 56,435,315-56,437,770 , GRCh37.p13 chr15: 56,727,513-56,729,968 TEX9, MNS1
    nsv6962611copy number variation1nstd229human GRCh38 chr15: 56,383,701-56,441,700 , GRCh37.p13 chr15: 56,675,899-56,733,898 MNS1, TEX9
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6622911copy number variation1nstd224human GRCh37 chr15: 56,748,680-56,874,924 , GRCh38.p12 chr15: 56,456,482-56,582,726 MNS1, LOC105370832
    nsv6589060inversion1nstd223human GRCh38 chr15: 56,442,601-56,448,564 , GRCh37.p13 chr15: 56,734,799-56,740,762 MNS1, TEX9
    nsv6514242copy number variation1nstd223human GRCh38 chr15: 56,401,833-56,566,829 , GRCh37.p13 chr15: 56,694,031-56,859,027 LOC105370832, TEX9, 1 more genes
    nsv6513179copy number variation1nstd223human GRCh38 chr15: 54,191,007-57,968,497 , GRCh37.p13 chr15: 54,483,204-58,260,695 HMGB1P33, LOC105370829, 43 more genes
    nsv6512211copy number variation1nstd223human GRCh38 chr15: 56,439,625-56,440,021 , GRCh37.p13 chr15: 56,731,823-56,732,219 TEX9, MNS1
    nsv6512114copy number variation1nstd223human GRCh38 chr15: 56,432,462-56,439,217 , GRCh37.p13 chr15: 56,724,660-56,731,415 TEX9, MNS1
    nsv6507171copy number variation1nstd223human GRCh38 chr15: 56,455,701-56,457,400 , GRCh37.p13 chr15: 56,747,899-56,749,598 MNS1
    nsv6506846copy number variation1nstd223human GRCh38 chr15: 56,446,201-56,447,700 , GRCh37.p13 chr15: 56,738,399-56,739,898 TEX9, MNS1
    nsv6500873copy number variation1nstd223human GRCh38 chr15: 56,429,215-56,429,504 , GRCh37.p13 chr15: 56,721,413-56,721,702 MNS1, TEX9
    nsv6497285copy number variation1nstd223human GRCh38 chr15: 56,444,378-56,444,903 , GRCh37.p13 chr15: 56,736,576-56,737,101 TEX9, MNS1
    nsv6497078copy number variation1nstd223human GRCh38 chr15: 56,370,901-56,541,500 , GRCh37.p13 chr15: 56,663,099-56,833,698 LOC105370832, MNS1, 1 more genes
    nsv6291481copy number variation1nstd102humanPathogenic GRCh37 chr15: 55,772,371-57,880,518 , GRCh38.p12 chr15: 55,480,173-57,588,320 PRTG, LOC390586, 27 more genes
    nsv6242124mobile element insertion1nstd215human GRCh38 chr15: 56,449,327-56,449,327 , GRCh37.p13 chr15: 56,741,525-56,741,525 MNS1
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