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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096244copy number variation1nstd102humanUncertain significance GRCh37 chr2: 227,659,726-228,567,034 , GRCh38.p12 chr2: 226,795,010-227,702,318 SLC19A3, IRS1, 12 more genes
    nsv7047209inversion1nstd229human GRCh38 chr2: 222,803,564-227,992,948 , GRCh37.p13 chr2: 223,668,283-228,857,664 MFF, LOC100289117, 55 more genes
    nsv7045781inversion1nstd229human GRCh38 chr2: 226,619,501-227,899,799 , GRCh37.p13 chr2: 227,484,217-228,764,515 SLC19A3, IRS1, 19 more genes
    nsv7043640inversion1nstd229human GRCh38 chr2: 222,841,128-228,011,478 , GRCh37.p13 chr2: 223,705,846-228,876,194 MFF-DT, LOC105373905, 55 more genes
    nsv6697216copy number variation1nstd229human GRCh38 chr2: 227,374,420-227,385,997 , GRCh37.p13 chr2: 228,239,136-228,250,713 TM4SF20
    nsv6696709copy number variation1nstd229human GRCh38 chr2: 227,372,201-227,386,100 , GRCh37.p13 chr2: 228,236,917-228,250,816 TM4SF20
    nsv6696055copy number variation1nstd229human GRCh38 chr2: 227,365,991-227,368,302 , GRCh37.p13 chr2: 228,230,707-228,233,018 TM4SF20
    nsv6694771copy number variation1nstd229human GRCh38 chr2: 227,372,968-227,378,626 , GRCh37.p13 chr2: 228,237,684-228,243,342 TM4SF20
    nsv6691430copy number variation1nstd229human GRCh38 chr2: 227,365,979-227,370,151 , GRCh37.p13 chr2: 228,230,695-228,234,867 TM4SF20
    nsv6678700copy number variation1nstd229human GRCh38 chr2: 226,880,942-228,292,097 , GRCh37.p13 chr2: 227,745,658-229,156,813 LOC107985993, LOC100533842, 21 more genes
    nsv6635600copy number variation1nstd227human GRCh38.p12 chr2: 227,378,594-227,394,141 , GRCh37 chr2: 228,243,310-228,258,857 TM4SF20
    nsv6635462copy number variation1nstd227human GRCh38.p12 chr2: 227,378,594-227,393,572 , GRCh37 chr2: 228,243,310-228,258,288 TM4SF20
    nsv6634514copy number variation1nstd102humanBenign GRCh37 chr2: 228,235,697-228,244,023 , GRCh38.p12 chr2: 227,370,981-227,379,307 TM4SF20
    nsv6628063copy number variation1nstd224human GRCh37 chr2: 228,243,816-228,258,857 , GRCh38.p12 chr2: 227,379,100-227,394,141 TM4SF20
    nsv6628062copy number variation29nstd224human GRCh37 chr2: 228,243,816-228,254,272 , GRCh38.p12 chr2: 227,379,100-227,389,556 TM4SF20
    nsv6628061copy number variation1nstd224human GRCh37 chr2: 228,243,247-228,255,420 , GRCh38.p12 chr2: 227,378,531-227,390,704 TM4SF20
    nsv6628060copy number variation4nstd224human GRCh37 chr2: 228,241,621-228,257,359 , GRCh38.p12 chr2: 227,376,905-227,392,643 TM4SF20
    nsv6628059copy number variation1nstd224human GRCh37 chr2: 228,197,164-228,254,272 , GRCh38.p12 chr2: 227,332,448-227,389,556 TM4SF20, MFF, 1 more genes
    nsv6628005copy number variation1nstd224human GRCh37 chr2: 228,244,335-228,257,359 , GRCh38.p12 chr2: 227,379,619-227,392,643 TM4SF20
    nsv6628004copy number variation1nstd224human GRCh37 chr2: 228,241,621-228,258,980 , GRCh38.p12 chr2: 227,376,905-227,394,264 TM4SF20
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