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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7049500inversion1nstd229human GRCh38 chr2: 3,572,568-6,665,412 , GRCh37.p13 chr2: 3,620,158-6,805,544 LOC105373393, LOC112268411, 33 more genes
    nsv7046036inversion1nstd229human GRCh38 chr2: 3,570,134-6,661,034 , GRCh37.p13 chr2: 3,617,724-6,801,166 MIR7515, LOC112268411, 33 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
    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
    nsv6670807copy number variation1nstd229human GRCh38 chr2: 3,571,360-3,574,985 , GRCh37.p13 chr2: 3,618,950-3,622,575 RPS7
    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
    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
    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
    nsv6353612copy number variation1nstd223human GRCh38 chr2: 3,573,601-3,574,938 , GRCh37.p13 chr2: 3,621,191-3,622,528 RPS7
    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
    nsv6337654copy number variation1nstd223human GRCh38 chr2: 2,974,401-4,112,000 , GRCh37.p13 chr2: 2,978,173-4,159,591 GAPDHP48, RNASEH1-DT, 17 more genes
    nsv6336927copy number variation1nstd223human GRCh38 chr2: 3,549,757-3,586,886 , GRCh37.p13 chr2: 3,597,347-3,634,476 RPS7, RNASEH1-DT, 1 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313677copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,498,882-3,800,549 , GRCh38.p12 chr2: 3,495,111-3,752,959 LOC105373393, GAPDHP48, 8 more genes
    nsv6311403copy number variation2nstd102humanUncertain significance GRCh37 chr2: 3,391,395-3,691,708 , GRCh38.p12 chr2: 3,387,624-3,644,118 TMSB4XP2, TRAPPC12, 7 more genes
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