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Items: 1 to 20 of 526

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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
    nsv6817564copy number variation1nstd229human GRCh38 chr6: 129,616,872-129,678,623 , GRCh37.p13 chr6: 129,938,017-129,999,768 ARHGAP18
    nsv6813282copy number variation1nstd229human GRCh38 chr6: 129,637,129-129,641,004 , GRCh37.p13 chr6: 129,958,274-129,962,149 ARHGAP18
    nsv6812825copy number variation1nstd229human GRCh38 chr6: 129,688,757-129,693,200 , GRCh37.p13 chr6: 130,009,902-130,014,345 ARHGAP18
    nsv6811141copy number variation1nstd229human GRCh38 chr6: 129,680,559-129,680,666 , GRCh37.p13 chr6: 130,001,704-130,001,811 ARHGAP18
    nsv6811009copy number variation1nstd229human GRCh38 chr6: 129,554,624-129,608,925 , GRCh37.p13 chr6: 129,875,769-129,930,070 ARHGAP18, LOC102723409
    nsv6810652copy number variation1nstd229human GRCh38 chr6: 129,632,510-129,758,394 , GRCh37.p13 chr6: 129,953,655-130,079,539 RPL5P21, ARHGAP18
    nsv6810301copy number variation1nstd229human GRCh38 chr6: 129,654,101-129,657,800 , GRCh37.p13 chr6: 129,975,246-129,978,945 ARHGAP18
    nsv6809273copy number variation1nstd229human GRCh38 chr6: 129,679,537-129,683,727 , GRCh37.p13 chr6: 130,000,682-130,004,872 ARHGAP18
    nsv6808963copy number variation1nstd229human GRCh38 chr6: 129,594,673-129,596,354 , GRCh37.p13 chr6: 129,915,818-129,917,499 ARHGAP18
    nsv6807420copy number variation1nstd229human GRCh38 chr6: 129,585,846-129,588,162 , GRCh37.p13 chr6: 129,906,991-129,909,307 ARHGAP18
    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
    nsv6803939copy number variation1nstd229human GRCh38 chr6: 129,700,085-129,700,202 , GRCh37.p13 chr6: 130,021,230-130,021,347 ARHGAP18
    nsv6803236copy number variation1nstd229human GRCh38 chr6: 129,696,596-129,697,329 , GRCh37.p13 chr6: 130,017,741-130,018,474 ARHGAP18
    nsv6802011copy number variation1nstd229human GRCh38 chr6: 129,694,737-129,701,682 , GRCh37.p13 chr6: 130,015,882-130,022,827 ARHGAP18
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