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Items: 1 to 20 of 28

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683029copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,547,614-109,547,794 , GRCh38.p12 chr12: 109,109,809-109,109,989 UNG
    nsv6309396copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,547,614-109,547,774 , GRCh38.p12 chr12: 109,109,809-109,109,969 UNG
    nsv4450869copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,547,614-109,547,794 , GRCh38 chr12: 109,109,809-109,109,989 UNG
    nsv3907255copy number variation1nstd102humanBenign GRCh37 chr12: 109,546,920-109,663,581 , GRCh38.p12 chr12: 109,109,115-109,225,776 UNG, LOC105369974, 1 more genes
    nsv3902715copy number variation1nstd102humanBenign GRCh37 chr12: 109,547,668-109,661,414 , GRCh38.p12 chr12: 109,109,863-109,223,609 UNG, LOC105369974, 1 more genes
    nsv3891598copy number variation1nstd102humanBenign GRCh37 chr12: 109,510,147-109,595,851 , GRCh38.p12 chr12: 109,072,342-109,158,046 UNG, ALKBH2, 3 more genes
    nsv3908651copy number variation1nstd102humanBenign GRCh37 chr12: 109,511,144-109,595,851 , GRCh38.p12 chr12: 109,073,339-109,158,046 UNG, LOC105369974, 3 more genes
    nsv3917474copy number variation1nstd102humanLikely benign GRCh37 chr12: 109,519,130-109,592,746 , GRCh38 chr12: 109,081,325-109,154,941 , NCBI36 chr12: 108,003,513-108,077,129 UNG, LOC105369974, 3 more genes
    nsv3904815copy number variation1nstd102humanBenign GRCh37 chr12: 109,509,250-109,582,205 , GRCh38.p12 chr12: 109,071,445-109,144,400 UNG, ACACB, 3 more genes
    nsv4457021copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,546,669-109,666,003 , GRCh38.p12 chr12: 109,108,864-109,228,198 UNG, ACACB, 1 more genes
    nsv5380892copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,547,614-109,665,314 , GRCh38.p12 chr12: 109,109,809-109,227,509 UNG, LOC105369974, 1 more genes
    nsv4455358copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,501,323-109,603,494 , GRCh38.p12 chr12: 109,063,518-109,165,689 UNG, LOC105369974, 3 more genes
    nsv4455641copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,502,471-109,595,474 , GRCh38.p12 chr12: 109,064,666-109,157,669 UNG, USP30, 3 more genes
    nsv6309459copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,535,485-109,577,883 , GRCh38.p12 chr12: 109,097,680-109,140,078 UNG, ACACB, 1 more genes
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 UNG, LOC105369964, 147 more genes
    nsv3916234copy number variation1nstd102humanPathogenic NCBI36 chr12: 104,152,585-111,116,873 , GRCh37 chr12: 105,628,455-112,632,490 , GRCh38 chr12: 105,234,677-112,194,686 UNG, LOC100287944, 141 more genes
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 UNG, ATP2A2, 115 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 UNG, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 UNG, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 UNG, RNU4ATAC16P, 2452 more genes
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