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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7046169inversion1nstd229human GRCh38 chr6: 129,271,276-130,554,936 , GRCh37.p13 chr6: 129,592,421-130,876,081 LOC105377999, ARHGAP18, 10 more genes
    nsv7038133inversion1nstd229human GRCh38 chr6: 129,535,207-129,868,832 , GRCh37.p13 chr6: 129,856,352-130,189,977 TMEM244, B3GALNT2P1, 4 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6811193copy number variation1nstd229human GRCh38 chr6: 129,813,067-129,887,898 , GRCh37.p13 chr6: 130,134,212-130,209,043 LOC105377999, TMEM244
    nsv6807634copy number variation1nstd229human GRCh38 chr6: 129,843,340-129,849,536 , GRCh37.p13 chr6: 130,164,485-130,170,681 TMEM244
    nsv6806364copy number variation1nstd229human GRCh38 chr6: 129,456,162-130,282,882 , GRCh37.p13 chr6: 129,777,307-130,604,027 LOC105377999, L3MBTL3, 7 more genes
    nsv6799801copy number variation1nstd229human GRCh38 chr6: 129,852,201-129,856,000 , GRCh37.p13 chr6: 130,173,346-130,177,145 LOC105377999, TMEM244
    nsv6634328complex substitution1nstd102humanPathogenic GRCh37 chr6: 129,604,517-130,268,447 , GRCh38.p12 chr6: 129,283,372-129,947,302 LAMA2, ARHGAP18, 6 more genes
    nsv6618676copy number variation1nstd223human GRCh38 chr6: 129,843,338-129,849,535 , GRCh37.p13 chr6: 130,164,483-130,170,680 TMEM244
    nsv6612236copy number variation1nstd223human GRCh38 chr6: 129,855,401-129,856,800 , GRCh37.p13 chr6: 130,176,546-130,177,945 LOC105377999, TMEM244
    nsv6608384copy number variation1nstd223human GRCh38 chr6: 129,841,601-129,844,000 , GRCh37.p13 chr6: 130,162,746-130,165,145 TMEM244
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6313508copy number variation1nstd102humanUncertain significance GRCh37 chr6: 129,779,876-130,603,406 , GRCh38.p12 chr6: 129,458,731-130,282,261 RPL5P21, L3MBTL3, 7 more genes
    nsv6136168copy number variation1nstd213human GRCh37 chr6: 130,130,000-130,280,001 , GRCh38.p12 chr6: 129,808,855-129,958,856 TMEM244, LOC105377999
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
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