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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063504inversion1nstd229human GRCh38 chr12: 118,107,799-118,588,852 , GRCh37.p13 chr12: 118,545,604-119,026,657 TAOK3, PEBP1, 3 more genes
    nsv6938018copy number variation1nstd229human GRCh38 chr12: 118,057,301-118,138,700 , GRCh37.p13 chr12: 118,495,106-118,576,505 LOC101928274, VSIG10, 2 more genes
    nsv6937205copy number variation1nstd229human GRCh38 chr12: 118,140,416-118,144,937 , GRCh37.p13 chr12: 118,578,221-118,582,742 PEBP1
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 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
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5506917copy number variation1nstd206human GRCh38 chr12: 118,137,755-118,141,140 , GRCh37.p13 chr12: 118,575,560-118,578,945 PEBP1
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4680133copy number variation1nstd189human GRCh37.p13 chr12: 118,431,926-118,855,845 , GRCh38.p12 chr12: 117,994,121-118,418,040 PEBP1, RFC5, 6 more genes
    nsv4675388copy number variation1nstd102humanUncertain significance GRCh37 chr12: 117,858,408-118,668,114 , GRCh38.p12 chr12: 117,420,603-118,230,309 LOC101928274, LOC105370012, 7 more genes
    nsv4617178copy number variation1nstd183human GRCh37 chr12: 118,561,298-118,584,117 , GRCh38.p12 chr12: 118,123,493-118,146,312 PEBP1, LOC101928274
    nsv4455668copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,718,607-119,728,623 , GRCh38.p12 chr12: 116,280,802-119,290,818 LINC00934, LOC105370019, 53 more genes
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3913894copy number variation1nstd102humanPathogenic NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902 TAOK3, LINC02405, 386 more genes
    nsv3906446copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 118,486,842-120,995,382 , GRCh38.p12 chr12: 118,049,037-120,557,579 COX6A1, MSI1, 63 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
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