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Items: 1 to 20 of 317

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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
    nsv7093381copy number variation1nstd102humannot provided GRCh37 chr6: 119,243,634-126,078,530 , GRCh38.p12 chr6: 118,922,469-125,757,384 HEY2-AS1, SERINC1, 52 more genes
    nsv7057554inversion1nstd229human GRCh38 chr6: 124,986,639-124,988,686 , GRCh37.p13 chr6: 125,307,785-125,309,832 RNF217
    nsv7051442inversion1nstd229human GRCh38 chr6: 120,525,437-125,245,762 , GRCh37.p13 chr6: 120,846,583-125,566,908 RNF217-AS1, HSF2, 35 more genes
    nsv7048775inversion1nstd229human GRCh38 chr6: 123,931,619-125,256,472 , GRCh37.p13 chr6: 124,252,764-125,577,618 RNF217-AS1, LOC100126584, 3 more genes
    nsv7042981inversion1nstd229human GRCh38 chr6: 122,939,434-128,158,341 , GRCh37.p13 chr6: 123,260,579-128,479,486 CENPW, VIM2P, 56 more genes
    nsv7038480inversion1nstd229human GRCh38 chr6: 124,998,212-125,006,158 , GRCh37.p13 chr6: 125,319,358-125,327,304 RNF217
    nsv6817028copy number variation1nstd229human GRCh38 chr6: 118,002,640-125,132,407 , GRCh37.p13 chr6: 118,323,803-125,453,553 GJA1, COX6A1P3, 56 more genes
    nsv6816933copy number variation1nstd229human GRCh38 chr6: 124,991,355-125,001,089 , GRCh37.p13 chr6: 125,312,501-125,322,235 RNF217
    nsv6815379copy number variation1nstd229human GRCh38 chr6: 125,039,273-125,044,885 , GRCh37.p13 chr6: 125,360,419-125,366,031 RNF217
    nsv6815313copy number variation1nstd229human GRCh38 chr6: 124,998,926-124,999,299 , GRCh37.p13 chr6: 125,320,072-125,320,445 RNF217
    nsv6815138copy number variation1nstd229human GRCh38 chr6: 125,077,932-125,078,051 , GRCh37.p13 chr6: 125,399,078-125,399,197 RNF217
    nsv6814436copy number variation1nstd229human GRCh38 chr6: 125,075,518-125,075,907 , GRCh37.p13 chr6: 125,396,664-125,397,053 RNF217
    nsv6814027copy number variation1nstd229human GRCh38 chr6: 124,969,874-124,969,904 , GRCh37.p13 chr6: 125,291,020-125,291,050 RNF217
    nsv6806582copy number variation1nstd229human GRCh38 chr6: 125,052,250-125,052,658 , GRCh37.p13 chr6: 125,373,396-125,373,804 RNF217
    nsv6804959copy number variation1nstd229human GRCh38 chr6: 124,990,162-124,993,463 , GRCh37.p13 chr6: 125,311,308-125,314,609 RNF217
    nsv6803322copy number variation1nstd229human GRCh38 chr6: 125,013,697-125,020,165 , GRCh37.p13 chr6: 125,334,843-125,341,311 RNF217
    nsv6802610copy number variation1nstd229human GRCh38 chr6: 125,049,643-125,049,673 , GRCh37.p13 chr6: 125,370,789-125,370,819 RNF217
    nsv6799252copy number variation1nstd229human GRCh38 chr6: 125,057,864-125,367,194 , GRCh37.p13 chr6: 125,379,010-125,688,340 TPD52L1, HDDC2, 4 more genes
    nsv6636864copy number variation1nstd102humanUncertain significance GRCh37 chr6: 120,059,951-130,033,233 , GRCh38.p12 chr6: 119,738,805-129,712,088 LOC107986640, ECHDC1, 93 more genes
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