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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3598868copy number variation1estd214human GRCh37 chr3: 180,200,419-180,206,004 , GRCh38.p12 chr3: 180,482,631-180,488,216 TTC14-DT
    esv3598872copy number variation1estd214human GRCh37 chr3: 180,275,476-180,279,407 , GRCh38.p12 chr3: 180,557,688-180,561,619 TTC14-DT
    esv3598870copy number variation1estd214human GRCh37 chr3: 180,250,804-180,253,874 , GRCh38.p12 chr3: 180,533,016-180,536,086 TTC14-DT
    esv3598871copy number variation35estd214human GRCh37 chr3: 180,262,785-180,263,250 , GRCh38.p12 chr3: 180,544,997-180,545,462 TTC14-DT
    esv3598869mobile element insertion9estd214human GRCh37 chr3: 180,232,397-180,232,397 , GRCh38.p12 chr3: 180,514,609-180,514,609 TTC14-DT
    nsv1014681copy number variation1nstd100human NCBI36 chr3: 173,711,933-195,388,187 , GRCh37.p13 chr3: 172,229,239-193,905,493 , GRCh38.p12 chr3: 172,511,449-194,187,704 , RTP1, 338 more genes
    nsv1012271copy number variation1nstd100human NCBI36 chr3: 181,289,569-181,717,565 , GRCh37.p13 chr3: 179,806,875-180,234,871 , GRCh38.p12 chr3: 180,089,087-180,517,083 GAPDHP36, LINC02053, 3 more genes
    nsv1012003copy number variation1nstd100human NCBI36 chr3: 156,657,937-199,255,755 , GRCh37.p13 chr3: 155,175,243-197,771,358 , GRCh38.p12 chr3: 155,457,454-198,044,487 , HES1, 684 more genes
    nsv1007831copy number variation1nstd100human NCBI36 chr3: 181,644,697-181,830,897 , GRCh37.p13 chr3: 180,162,003-180,348,203 , GRCh38.p12 chr3: 180,444,215-180,630,415 TTC14, TTC14-DT, 2 more genes
    nsv1001123copy number variation1nstd100human NCBI36 chr3: 155,486,736-199,255,755 , GRCh37.p13 chr3: 154,004,042-197,771,358 , GRCh38.p12 chr3: 154,286,253-198,044,487 , LOC102724808, 699 more genes
    esv3562985copy number variation1estd215human GRCh37 chr3: 180,294,402-180,295,560 , GRCh38.p12 chr3: 180,576,614-180,577,772 TTC14-DT
    esv3562984copy number variation1estd215human GRCh37 chr3: 180,231,991-180,232,040 , GRCh38.p12 chr3: 180,514,203-180,514,252 TTC14-DT
    nsv984837copy number variation2nstd11human GRCh37.p13 chr3: 60,345-197,896,118 , GRCh38.p12 chr3: 18,667-198,169,247 , NCBI36 chr3: 35,345-199,380,515 , AADAC, 2982 more genes
    esv3439885insertion1estd59human NCBI36 chr3: 181,715,015-181,715,192 , GRCh37.p13 chr3: 180,232,321-180,232,498 , GRCh38.p12 chr3: 180,514,533-180,514,710 TTC14-DT
    esv3393709copy number variation1estd59human NCBI36 chr3: 181,685,580-181,687,745 , GRCh37.p13 chr3: 180,202,886-180,205,051 , GRCh38.p12 chr3: 180,485,098-180,487,263 TTC14-DT
    esv3359190copy number variation1estd59human NCBI36 chr3: 181,781,090-181,879,917 , GRCh37.p13 chr3: 180,298,396-180,397,223 , GRCh38.p12 chr3: 180,580,608-180,679,435 TTC14, RNU6-486P, 2 more genes
    esv3342538copy number variation1estd59human NCBI36 chr3: 181,763,692-181,763,990 , GRCh37.p13 chr3: 180,280,998-180,281,296 , GRCh38.p12 chr3: 180,563,210-180,563,508 TTC14-DT
    esv3325922copy number variation2estd59human NCBI36 chr3: 181,696,802-181,696,902 , GRCh37.p13 chr3: 180,214,108-180,214,208 , GRCh38.p12 chr3: 180,496,320-180,496,420 TTC14-DT
    esv3306758mobile element insertion1estd59human NCBI36 chr3: 181,714,991-181,715,159 , GRCh37.p13 chr3: 180,232,297-180,232,465 , GRCh38.p12 chr3: 180,514,509-180,514,677 TTC14-DT
    esv3251375insertion1estd209human GRCh37 chr3: 180,272,131-180,272,131 , GRCh38.p12 chr3: 180,554,343-180,554,343 TTC14-DT
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