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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7096639copy number variation2nstd102humanUncertain significance GRCh37 chr2: 44,001,278-44,209,593 , GRCh38.p12 chr2: 43,774,139-43,982,454 LOC105374571, RNU6-1048P, 6 more genes
    nsv7096160copy number variation1nstd102humanUncertain significance GRCh37 chr2: 44,047,034-44,047,259 , GRCh38.p12 chr2: 43,819,895-43,820,120 DYNC2LI1, ABCG5
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6677615copy number variation1nstd229human GRCh38 chr2: 43,817,923-43,901,048 , GRCh37.p13 chr2: 44,045,062-44,128,187 LRPPRC, ABCG5, 4 more genes
    nsv6676797copy number variation1nstd229human GRCh38 chr2: 43,763,317-44,075,069 , GRCh37.p13 chr2: 43,990,456-44,302,208 ABCG8, LOC102725159, 8 more genes
    nsv6676342copy number variation1nstd229human GRCh38 chr2: 43,813,601-43,849,200 , GRCh37.p13 chr2: 44,040,740-44,076,339 ABCG5, ABCG8, 2 more genes
    nsv6672004copy number variation1nstd229human GRCh38 chr2: 43,785,555-43,804,955 , GRCh37.p13 chr2: 44,012,694-44,032,094 ABCG5, DYNC2LI1
    nsv6669625copy number variation1nstd229human GRCh38 chr2: 43,704,962-43,967,130 , GRCh37.p13 chr2: 43,932,101-44,194,269 LOC105374571, RNU6-1048P, 8 more genes
    nsv6668305copy number variation1nstd229human GRCh38 chr2: 43,827,059-43,827,624 , GRCh37.p13 chr2: 44,054,198-44,054,763 ABCG5, DYNC2LI1
    nsv6667571copy number variation1nstd229human GRCh38 chr2: 43,824,420-43,824,465 , GRCh37.p13 chr2: 44,051,559-44,051,604 ABCG5, DYNC2LI1
    nsv6667408copy number variation1nstd229human GRCh38 chr2: 43,799,250-43,890,984 , GRCh37.p13 chr2: 44,026,389-44,118,123 ABCG5, LRPPRC, 4 more genes
    nsv6665468copy number variation1nstd229human GRCh38 chr2: 43,804,135-43,806,475 , GRCh37.p13 chr2: 44,031,274-44,033,614 ABCG5, DYNC2LI1
    nsv6664648copy number variation1nstd229human GRCh38 chr2: 43,506,633-43,999,710 , GRCh37.p13 chr2: 43,733,772-44,226,849 DYNC2LI1, ABCG8, 11 more genes
    nsv6663614copy number variation1nstd229human GRCh38 chr2: 43,836,439-43,840,223 , GRCh37.p13 chr2: 44,063,578-44,067,362 ABCG8, ABCG5
    nsv6663051copy number variation1nstd229human GRCh38 chr2: 43,825,245-43,833,668 , GRCh37.p13 chr2: 44,052,384-44,060,807 ABCG8, DYNC2LI1, 1 more genes
    nsv6661808copy number variation1nstd229human GRCh38 chr2: 43,825,801-44,133,280 , GRCh37.p13 chr2: 44,052,940-44,360,419 ABCG5, DYNC2LI1, 5 more genes
    nsv6661474copy number variation1nstd229human GRCh38 chr2: 43,782,955-44,013,202 , GRCh37.p13 chr2: 44,010,094-44,240,341 LOC102725159, RNU6-1048P, 5 more genes
    nsv6658992copy number variation1nstd229human GRCh38 chr2: 43,832,999-43,833,576 , GRCh37.p13 chr2: 44,060,138-44,060,715 ABCG5, ABCG8
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
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