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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146572insertion1nstd232human GRCh37.p13 chr11: 86,018,382-86,018,382 , GRCh38.p12 chr11: 86,307,340-86,307,340 HIKESHI
    nsv7142948insertion1nstd232human GRCh37.p13 chr11: 86,019,209-86,019,209 , GRCh38.p12 chr11: 86,308,167-86,308,167 HIKESHI
    nsv7094112copy number variation1nstd102humanUncertain significance GRCh37 chr11: 86,013,491-86,013,540 , GRCh38.p12 chr11: 86,302,449-86,302,498 HIKESHI
    nsv7094111copy number variation1nstd102humanPathogenic GRCh37 chr11: 85,339,652-86,666,127 , GRCh38.p12 chr11: 85,628,608-86,955,085 PRSS23, OR7E13P, 30 more genes
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv7068892inversion1nstd229human GRCh38 chr11: 85,482,651-87,653,297 , GRCh37.p13 chr11: 85,193,695-87,364,189 , RNU6-1292P, 42 more genes
    nsv7063328inversion1nstd229human GRCh38 chr11: 86,096,439-87,353,928 , GRCh37.p13 chr11: 85,807,481-87,064,970 , PRSS23, 28 more genes
    nsv7062832inversion1nstd229human GRCh38 chr11: 86,269,753-86,303,085 , GRCh37.p13 chr11: 85,980,795-86,014,127 EED, HIKESHI, 3 more genes
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv6917860copy number variation1nstd229human GRCh38 chr11: 86,330,284-86,330,481 , GRCh37.p13 chr11: 86,041,326-86,041,523 HIKESHI
    nsv6915425copy number variation1nstd229human GRCh38 chr11: 86,341,824-86,341,991 , GRCh37.p13 chr11: 86,052,866-86,053,033 HIKESHI, LOC105369421
    nsv6912307copy number variation1nstd229human GRCh38 chr11: 86,326,888-86,327,302 , GRCh37.p13 chr11: 86,037,930-86,038,344 HIKESHI
    nsv6907517copy number variation1nstd229human GRCh38 chr11: 86,296,501-86,301,000 , GRCh37.p13 chr11: 86,007,543-86,012,042 HIKESHI
    nsv6905543copy number variation1nstd229human GRCh38 chr11: 84,763,504-86,648,143 , GRCh37.p13 chr11: 84,474,547-86,359,185 CCDC83, CCDC81, 25 more genes
    nsv6905042copy number variation1nstd229human GRCh38 chr11: 86,309,201-86,313,700 , GRCh37.p13 chr11: 86,020,243-86,024,742 HIKESHI
    nsv6901829copy number variation1nstd229human GRCh38 chr11: 86,326,499-86,332,969 , GRCh37.p13 chr11: 86,037,541-86,044,011 HIKESHI
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6588685inversion1nstd223human GRCh38 chr11: 86,313,393-86,314,453 , GRCh37.p13 chr11: 86,024,435-86,025,495 HIKESHI
    nsv6587964inversion1nstd223human GRCh38 chr11: 86,320,543-86,320,957 , GRCh37.p13 chr11: 86,031,585-86,031,999 HIKESHI
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