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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6992491copy number variation1nstd229human GRCh38 chr16: 49,465,522-49,465,581 , GRCh37.p13 chr16: 49,499,433-49,499,492 LINC02179
    nsv6991369copy number variation1nstd229human GRCh38 chr16: 49,464,074-49,466,549 , GRCh37.p13 chr16: 49,497,985-49,500,460 LINC02179
    nsv6990999copy number variation1nstd229human GRCh38 chr16: 49,458,390-49,467,283 , GRCh37.p13 chr16: 49,492,301-49,501,194 LINC02179
    nsv6982398copy number variation1nstd229human GRCh38 chr16: 49,432,901-50,109,800 , GRCh37.p13 chr16: 49,466,812-50,143,711 CNEP1R1, ADAM3B, 10 more genes
    nsv6978249copy number variation1nstd229human GRCh38 chr16: 49,469,313-49,478,043 , GRCh37.p13 chr16: 49,503,224-49,511,954 LINC02179
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6502793copy number variation1nstd223human GRCh38 chr16: 49,464,072-49,466,546 , GRCh37.p13 chr16: 49,497,983-49,500,457 LINC02179
    nsv6501365copy number variation1nstd223human GRCh38 chr16: 49,469,078-49,470,594 , GRCh37.p13 chr16: 49,502,989-49,504,505 LINC02179
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6195002copy number variation1nstd214human GRCh38 chr16: 49,465,522-49,465,580 , GRCh37.p13 chr16: 49,499,433-49,499,491 LINC02179
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6033295copy number variation1nstd212human GRCh38 chr16: 49,465,522-49,465,581 , GRCh37.p13 chr16: 49,499,433-49,499,492 LINC02179
    nsv5934309copy number variation1nstd209human GRCh38 chr16: 49,465,522-49,465,580 , GRCh37.p13 chr16: 49,499,433-49,499,491 LINC02179
    nsv5592677copy number variation1nstd207human GRCh38 chr16: 49,465,522-49,465,580 , GRCh37.p13 chr16: 49,499,433-49,499,491 LINC02179
    nsv5518777copy number variation1nstd206human GRCh38 chr16: 49,465,527-49,465,581 , GRCh37.p13 chr16: 49,499,438-49,499,492 LINC02179
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4680405copy number variation1nstd189human GRCh37.p13 chr16: 49,422,792-49,644,803 , GRCh38.p12 chr16: 49,388,881-49,610,892 , ADAM3B, 4 more genes
    nsv4675028copy number variation1nstd102humanUncertain significance GRCh37 chr16: 49,469,515-49,961,548 , GRCh38.p12 chr16: 49,435,604-49,927,637 LOC105371244, MRPS21P8, 4 more genes
    nsv4654854copy number variation1nstd186human GRCh37 chr16: 49,499,434-49,499,492 , GRCh38.p12 chr16: 49,465,523-49,465,581 LINC02179
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