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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6937005copy number variation1nstd229human GRCh38 chr12: 120,465,601-120,774,200 , GRCh37.p13 chr12: 120,903,404-121,212,003 DYNLL1, RNF10, 14 more genes
    nsv6935422copy number variation1nstd229human GRCh38 chr12: 120,465,701-120,471,600 , GRCh37.p13 chr12: 120,903,504-120,909,403 SRSF9, DYNLL1
    nsv6935163copy number variation1nstd229human GRCh38 chr12: 120,067,201-120,694,800 , GRCh37.p13 chr12: 120,505,005-121,132,603 RPL11P5, RNF10, 30 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934467copy number variation1nstd229human GRCh38 chr12: 120,407,101-120,775,400 , GRCh37.p13 chr12: 120,844,904-121,213,203 SPPL3, RPL31P52, 18 more genes
    nsv6930227copy number variation1nstd229human GRCh38 chr12: 120,250,901-120,560,500 , GRCh37.p13 chr12: 120,688,704-120,998,303 RNU6-1088P, RNF10, 17 more genes
    nsv6930083copy number variation1nstd229human GRCh38 chr12: 120,251,001-120,606,400 , GRCh37.p13 chr12: 120,688,804-121,044,203 COX6A1, NRAV, 19 more genes
    nsv6923564copy number variation1nstd229human GRCh38 chr12: 120,470,101-120,477,300 , GRCh37.p13 chr12: 120,907,904-120,915,103 SRSF9, DYNLL1
    nsv6920986copy number variation1nstd229human GRCh38 chr12: 120,439,940-120,461,480 , GRCh37.p13 chr12: 120,877,743-120,899,283 TRIAP1, COX6A1, 3 more genes
    nsv6919599copy number variation1nstd229human GRCh38 chr12: 119,989,801-120,740,500 , GRCh37.p13 chr12: 120,427,605-121,178,303 RPS20P31, MLEC, 33 more genes
    nsv6637895copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,665,945-120,951,612 , GRCh38.p12 chr12: 120,228,142-120,513,809 SIRT4, RPS20P31, 16 more genes
    nsv6637490copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,761,046-121,280,839 , GRCh38.p12 chr12: 120,323,243-120,843,036 RPS27P25, MIR4700, 22 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6480154copy number variation1nstd223human GRCh38 chr12: 120,443,739-120,459,806 , GRCh37.p13 chr12: 120,881,542-120,897,609 SRSF9, TRIAP1, 2 more genes
    nsv6476788copy number variation1nstd223human GRCh38 chr12: 120,442,140-121,624,181 , GRCh37.p13 chr12: 120,879,943-121,761,800 RNU6-1004P, LOC105370030, 39 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6143905copy number variation1nstd206human GRCh38 chr12: 120,454,128-120,460,128 , GRCh37.p13 chr12: 120,891,931-120,897,931 GATC, SRSF9
    nsv6097731insertion1nstd212human GRCh38 chr12: 120,467,996-120,467,996 , GRCh37.p13 chr12: 120,905,799-120,905,799 SRSF9, DYNLL1
    nsv6033354copy number variation1nstd212human GRCh38 chr12: 120,467,823-120,468,110 , GRCh37.p13 chr12: 120,905,626-120,905,913 DYNLL1, SRSF9
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
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