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Items: 1 to 20 of 495

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6817425copy number variation1nstd229human GRCh38 chr6: 97,153,706-97,153,881 , GRCh37.p13 chr6: 97,601,582-97,601,757 MMS22L
    nsv6817411copy number variation1nstd229human GRCh38 chr6: 97,154,141-97,320,309 , GRCh37.p13 chr6: 97,602,017-97,768,185 MMS22L, LOC101927314
    nsv6816974copy number variation1nstd229human GRCh38 chr6: 97,277,269-97,329,504 , GRCh37.p13 chr6: 97,725,145-97,777,380 MMS22L, LOC101927314
    nsv6813541copy number variation1nstd229human GRCh38 chr6: 97,029,298-97,250,140 , GRCh37.p13 chr6: 97,477,174-97,698,016 KLHL32, MMS22L
    nsv6812462copy number variation1nstd229human GRCh38 chr6: 97,187,074-97,356,108 , GRCh37.p13 chr6: 97,634,950-97,803,984 LOC101927314, MMS22L
    nsv6808570copy number variation1nstd229human GRCh38 chr6: 97,189,733-97,189,772 , GRCh37.p13 chr6: 97,637,609-97,637,648 MMS22L
    nsv6808087copy number variation1nstd229human GRCh38 chr6: 97,152,799-97,153,162 , GRCh37.p13 chr6: 97,600,675-97,601,038 MMS22L
    nsv6807330copy number variation1nstd229human GRCh38 chr6: 97,242,296-97,245,605 , GRCh37.p13 chr6: 97,690,172-97,693,481 MMS22L
    nsv6806362copy number variation1nstd229human GRCh38 chr6: 97,193,310-97,199,125 , GRCh37.p13 chr6: 97,641,186-97,647,001 MMS22L
    nsv6805794copy number variation1nstd229human GRCh38 chr6: 97,274,693-97,639,144 , GRCh37.p13 chr6: 97,722,569-98,087,020 LOC107986627, LOC101927314, 2 more genes
    nsv6804363copy number variation1nstd229human GRCh38 chr6: 97,281,011-97,291,351 , GRCh37.p13 chr6: 97,728,887-97,739,227 MMS22L
    nsv6803960copy number variation1nstd229human GRCh38 chr6: 97,161,527-97,169,469 , GRCh37.p13 chr6: 97,609,403-97,617,345 MMS22L
    nsv6799564copy number variation1nstd229human GRCh38 chr6: 97,254,394-97,254,490 , GRCh37.p13 chr6: 97,702,270-97,702,366 MMS22L
    nsv6799548copy number variation1nstd229human GRCh38 chr6: 97,179,358-97,287,128 , GRCh37.p13 chr6: 97,627,234-97,735,004 MMS22L
    nsv6798505copy number variation1nstd229human GRCh38 chr6: 97,191,452-97,191,578 , GRCh37.p13 chr6: 97,639,328-97,639,454 MMS22L
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631277copy number variation1nstd224human GRCh37 chr6: 95,390,186-97,681,784 , GRCh38.p12 chr6: 94,680,468-97,233,908 NDUFAF4, MANEA, 21 more genes
    nsv6619424copy number variation1nstd223human GRCh38 chr6: 97,208,387-97,212,795 , GRCh37.p13 chr6: 97,656,263-97,660,671 MMS22L
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