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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096638copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,599,714-3,605,850 , GRCh38.p12 chr2: 3,552,124-3,558,260 RNASEH1-DT, RNASEH1
    nsv7096158copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,391,395-3,624,240 , GRCh38.p12 chr2: 3,387,624-3,576,650 , GRCh38.p12 chr2|NT_187522.1: 1-120,616 RPS7, RNASEH1-DT, 4 more genes
    nsv7057382inversion1nstd229human GRCh38 chr2: 3,343,573-5,044,013 , GRCh37.p13 chr2: 3,347,344-5,184,146 RNASEH1-DT, LOC105373394, 19 more genes
    nsv7045549inversion1nstd229human GRCh38 chr2: 2,958,160-3,653,889 , GRCh37.p13 chr2: 2,961,932-3,701,479 EIPR1, RPS7, 10 more genes
    nsv7039393inversion1nstd229human GRCh38 chr2: 378,067-4,298,462 , GRCh37.p13 chr2: 378,067-4,346,052 LOC105373393, RPS7, 42 more genes
    nsv6675070copy number variation1nstd229human GRCh38 chr2: 3,532,642-3,542,213 , GRCh37.p13 chr2: 3,580,232-3,589,803 RNASEH1
    nsv6673170copy number variation1nstd229human GRCh38 chr2: 3,418,301-3,651,400 , GRCh37.p13 chr2: 3,422,072-3,698,990 RNASEH1, ALLC, 7 more genes
    nsv6672744copy number variation1nstd229human GRCh38 chr2: 3,551,411-3,560,940 , GRCh37.p13 chr2: 3,599,001-3,608,530 RNASEH1-DT, RNASEH1
    nsv6669294copy number variation1nstd229human GRCh38 chr2: 3,533,068-3,533,427 , GRCh37.p13 chr2: 3,580,658-3,581,017 RNASEH1
    nsv6667193copy number variation1nstd229human GRCh38 chr2: 3,358,584-3,733,752 , GRCh37.p13 chr2: 3,362,355-3,781,342 GAPDHP48, RNASEH1-DT, 11 more genes
    nsv6666353copy number variation1nstd229human GRCh38 chr2: 3,533,830-3,533,930 , GRCh37.p13 chr2: 3,581,420-3,581,520 RNASEH1
    nsv6660902copy number variation1nstd229human GRCh38 chr2: 3,357,717-4,915,960 , GRCh37.p13 chr2: 3,361,488-4,963,550 COLEC11, LOC105373397, 18 more genes
    nsv6659826copy number variation1nstd229human GRCh38 chr2: 3,468,034-3,705,601 , GRCh37.p13 chr2: 3,471,805-3,753,191 RNASEH1-DT, ADI1, 10 more genes
    nsv6658249copy number variation1nstd229human GRCh38 chr2: 3,558,101-3,559,800 , GRCh37.p13 chr2: 3,605,691-3,607,390 RNASEH1, RNASEH1-DT
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6628051copy number variation1nstd224human GRCh37 chr2: 3,066,698-4,076,520 , GRCh38.p12 chr2: 3,062,926-4,028,930 EIPR1, DCDC2C, 16 more genes
    nsv6549472inversion1nstd223human GRCh38 chr2: 3,540,692-3,541,321 , GRCh37.p13 chr2: 3,588,282-3,588,911 RNASEH1
    nsv6540561inversion1nstd223human GRCh38 chr2: 3,556,163-3,556,437 , GRCh37.p13 chr2: 3,603,753-3,604,027 RNASEH1-DT, RNASEH1
    nsv6344958copy number variation1nstd223human GRCh38 chr2: 3,530,365-3,531,136 , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv6342464copy number variation1nstd223human GRCh38 chr2: 3,358,584-3,733,752 , GRCh37.p13 chr2: 3,362,355-3,781,342 RNASEH1, EIPR1, 11 more genes
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