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Items: 1 to 20 of 579

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112707copy number variation1nstd102humanUncertain significance GRCh38 chr1: 6,234,122-6,508,845 , GRCh37.p13 chr1: 6,294,182-6,568,905 HES3, PLEKHG5, 8 more genes
    nsv6112685copy number variation1nstd102humannot provided GRCh37 chr1: 2,420,003-8,155,935 , GRCh38.p12 chr1: 2,488,564-8,095,875 LINC02780, C1orf174, 100 more genes
    nsv5960000insertion1nstd209human GRCh38 chr1: 6,381,867-6,381,867 , GRCh37.p13 chr1: 6,441,927-6,441,927 ACOT7
    nsv5887158copy number variation1nstd209human GRCh38 chr1: 6,381,853-6,382,131 , GRCh37.p13 chr1: 6,441,913-6,442,191 ACOT7
    nsv5886151copy number variation1nstd209human GRCh38 chr1: 6,305,699-6,305,774 , GRCh37.p13 chr1: 6,365,759-6,365,834 ACOT7
    nsv5872489copy number variation1nstd209human GRCh38 chr1: 6,378,109-6,385,834 , GRCh37.p13 chr1: 6,438,169-6,445,894 ACOT7
    nsv5869311copy number variation1nstd209human GRCh38 chr1: 6,300,461-6,300,521 , GRCh37.p13 chr1: 6,360,521-6,360,581 ACOT7
    nsv5867909copy number variation1nstd209human GRCh38 chr1: 6,307,828-6,307,887 , GRCh37.p13 chr1: 6,367,888-6,367,947 ACOT7
    nsv5830722copy number variation1nstd209human GRCh38 chr1: 6,378,178-6,385,853 , GRCh37.p13 chr1: 6,438,238-6,445,913 ACOT7
    nsv5720391mobile element insertion2nstd211human GRCh38 chr1: 6,338,000-6,338,000 , GRCh37.p13 chr1: 6,398,060-6,398,060 ACOT7
    nsv5680477mobile element insertion1nstd211human GRCh38 chr1: 6,303,478-6,303,478 , GRCh37.p13 chr1: 6,363,538-6,363,538 ACOT7
    nsv5613719insertion1nstd207human GRCh38 chr1: 6,300,756-6,300,756 , GRCh37.p13 chr1: 6,360,816-6,360,816 ACOT7
    nsv5609477insertion1nstd207human GRCh38 chr1: 6,354,670-6,354,670 , GRCh37.p13 chr1: 6,414,730-6,414,730 ACOT7
    nsv5573147copy number variation1nstd207human GRCh38 chr1: 6,308,151-6,308,302 , GRCh37.p13 chr1: 6,368,211-6,368,362 ACOT7
    nsv5569786copy number variation1nstd207human GRCh38 chr1: 6,304,648-6,306,100 , GRCh37.p13 chr1: 6,364,708-6,366,160 ACOT7
    nsv5569599copy number variation1nstd207human GRCh38 chr1: 6,378,109-6,385,834 , GRCh37.p13 chr1: 6,438,169-6,445,894 ACOT7
    nsv5568246copy number variation1nstd207human GRCh38 chr1: 6,305,129-6,305,304 , GRCh37.p13 chr1: 6,365,189-6,365,364 ACOT7
    nsv5557666sequence alteration1nstd206human GRCh38 chr1: 6,304,536-6,306,133 , GRCh37.p13 chr1: 6,364,596-6,366,193 ACOT7
    nsv5433221copy number variation1nstd206human GRCh38 chr1: 6,260,738-6,262,525 , GRCh37.p13 chr1: 6,320,798-6,322,585 ACOT7, GPR153
    nsv5428397copy number variation1nstd206human GRCh38 chr1: 6,393,044-6,393,110 , GRCh37.p13 chr1: 6,453,104-6,453,170 ACOT7
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