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Items: 1 to 20 of 518

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6976196copy number variation1nstd229human GRCh38 chr15: 58,693,085-58,695,734 , GRCh37.p13 chr15: 58,985,284-58,987,933 ADAM10, HSP90AB4P
    nsv6976073copy number variation1nstd229human GRCh38 chr15: 58,690,126-58,692,737 , GRCh37.p13 chr15: 58,982,325-58,984,936 ADAM10, HSP90AB4P
    nsv6976072copy number variation1nstd229human GRCh38 chr15: 58,601,546-58,601,583 , GRCh37.p13 chr15: 58,893,745-58,893,782 ADAM10
    nsv6974594copy number variation1nstd229human GRCh38 chr15: 58,621,731-58,622,007 , GRCh37.p13 chr15: 58,913,930-58,914,206 ADAM10
    nsv6974073copy number variation1nstd229human GRCh38 chr15: 58,744,312-58,748,263 , GRCh37.p13 chr15: 59,036,511-59,040,462 ADAM10
    nsv6973728copy number variation1nstd229human GRCh38 chr15: 58,677,476-58,677,787 , GRCh37.p13 chr15: 58,969,675-58,969,986 ADAM10
    nsv6972147copy number variation1nstd229human GRCh38 chr15: 58,612,142-58,612,328 , GRCh37.p13 chr15: 58,904,341-58,904,527 ADAM10
    nsv6971230copy number variation1nstd229human GRCh38 chr15: 58,620,649-58,620,967 , GRCh37.p13 chr15: 58,912,848-58,913,166 ADAM10
    nsv6967866copy number variation1nstd229human GRCh38 chr15: 58,667,075-58,671,026 , GRCh37.p13 chr15: 58,959,274-58,963,225 ADAM10, HMGB1P51
    nsv6967782copy number variation1nstd229human GRCh38 chr15: 58,694,414-58,694,828 , GRCh37.p13 chr15: 58,986,613-58,987,027 ADAM10
    nsv6967423copy number variation1nstd229human GRCh38 chr15: 58,707,307-58,715,346 , GRCh37.p13 chr15: 58,999,506-59,007,545 ADAM10
    nsv6963018copy number variation1nstd229human GRCh38 chr15: 58,717,433-58,717,783 , GRCh37.p13 chr15: 59,009,632-59,009,982 ADAM10
    nsv6962280copy number variation1nstd229human GRCh38 chr15: 58,648,269-58,661,480 , GRCh37.p13 chr15: 58,940,468-58,953,679 ADAM10
    nsv6960566copy number variation1nstd229human GRCh38 chr15: 58,692,555-58,696,003 , GRCh37.p13 chr15: 58,984,754-58,988,202 HSP90AB4P, ADAM10
    nsv6960014copy number variation1nstd229human GRCh38 chr15: 58,720,301-58,724,400 , GRCh37.p13 chr15: 59,012,500-59,016,599 ADAM10
    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
    nsv6593469inversion1nstd223human GRCh38 chr15: 58,659,028-58,659,779 , GRCh37.p13 chr15: 58,951,227-58,951,978 ADAM10
    nsv6590170inversion1nstd223human GRCh38 chr15: 58,642,473-58,644,527 , GRCh37.p13 chr15: 58,934,672-58,936,726 ADAM10
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