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Items: 1 to 20 of 225

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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
    nsv7054215inversion1nstd229human GRCh38 chr6: 124,948,602-124,948,700 , GRCh37.p13 chr6: 125,269,748-125,269,846 RNF217-AS1
    nsv7051442inversion1nstd229human GRCh38 chr6: 120,525,437-125,245,762 , GRCh37.p13 chr6: 120,846,583-125,566,908 RNF217-AS1, HSF2, 35 more genes
    nsv7050574inversion1nstd229human GRCh38 chr6: 124,908,513-124,908,529 , GRCh37.p13 chr6: 125,229,659-125,229,675 RNF217-AS1
    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
    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
    nsv6806287copy number variation1nstd229human GRCh38 chr6: 124,909,171-124,921,148 , GRCh37.p13 chr6: 125,230,317-125,242,294 RNF217-AS1
    nsv6803213copy number variation1nstd229human GRCh38 chr6: 124,947,301-124,958,600 , GRCh37.p13 chr6: 125,268,447-125,279,746 RNF217-AS1
    nsv6801440copy number variation1nstd229human GRCh38 chr6: 124,909,149-124,913,220 , GRCh37.p13 chr6: 125,230,295-125,234,366 RNF217-AS1
    nsv6801119copy number variation1nstd229human GRCh38 chr6: 124,901,049-124,910,532 , GRCh37.p13 chr6: 125,222,195-125,231,678 RNF217-AS1
    nsv6798755copy number variation1nstd229human GRCh38 chr6: 124,463,844-124,956,498 , GRCh37.p13 chr6: 124,784,990-125,277,644 NKAIN2, RNF217-AS1
    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
    nsv6636829copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,858,348-125,320,485 , GRCh38.p12 chr6: 123,537,203-124,999,339 TRDN, NKAIN2, 4 more genes
    nsv6611343copy number variation1nstd223human GRCh38 chr6: 124,909,149-124,913,216 , GRCh37.p13 chr6: 125,230,295-125,234,362 RNF217-AS1
    nsv6610376copy number variation1nstd223human GRCh38 chr6: 124,955,186-124,955,678 , GRCh37.p13 chr6: 125,276,332-125,276,824 RNF217-AS1
    nsv6607878copy number variation1nstd223human GRCh38 chr6: 124,939,905-124,940,503 , GRCh37.p13 chr6: 125,261,051-125,261,649 RNF217-AS1
    nsv6606291copy number variation1nstd223human GRCh38 chr6: 124,913,214-125,239,682 , GRCh37.p13 chr6: 125,234,360-125,560,828 LOC100126584, RNF217, 2 more genes
    nsv6603019copy number variation1nstd223human GRCh38 chr6: 124,952,205-124,952,774 , GRCh37.p13 chr6: 125,273,351-125,273,920 RNF217-AS1
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