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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995942copy number variation1nstd229human GRCh38 chr17: 55,389,589-55,391,442 , GRCh37.p13 chr17: 53,466,950-53,468,803 MMD
    nsv6986495copy number variation1nstd229human GRCh38 chr17: 55,406,106-55,406,132 , GRCh37.p13 chr17: 53,483,467-53,483,493 MMD
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6982420copy number variation1nstd229human GRCh38 chr17: 55,392,701-55,402,300 , GRCh37.p13 chr17: 53,470,062-53,479,661 MMD
    nsv6534570copy number variation1nstd223human GRCh38 chr17: 55,407,973-55,408,481 , GRCh37.p13 chr17: 53,485,334-53,485,842 MMD
    nsv6526215copy number variation1nstd223human GRCh38 chr17: 55,409,951-55,412,022 , GRCh37.p13 chr17: 53,487,312-53,489,383 MMD
    nsv6525114copy number variation1nstd223human GRCh38 chr17: 55,391,511-55,392,017 , GRCh37.p13 chr17: 53,468,872-53,469,378 MMD
    nsv6522457copy number variation1nstd223human GRCh38 chr17: 55,399,324-55,409,668 , GRCh37.p13 chr17: 53,476,685-53,487,029 MMD
    nsv6517041copy number variation1nstd223human GRCh38 chr17: 55,421,001-55,422,500 , GRCh37.p13 chr17: 53,498,362-53,499,861 MMD
    nsv6286598insertion1nstd214human GRCh38 chr17: 55,405,690-55,405,690 , GRCh37.p13 chr17: 53,483,051-53,483,051 MMD
    nsv5709277mobile element insertion2nstd211human GRCh38 chr17: 55,393,985-55,393,985 , GRCh37.p13 chr17: 53,471,346-53,471,346 MMD
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5533760copy number variation1nstd206human GRCh38 chr17: 55,407,449-55,407,509 , GRCh37.p13 chr17: 53,484,810-53,484,870 MMD
    nsv5529141copy number variation1nstd206human GRCh38 chr17: 55,396,760-55,397,264 , GRCh37.p13 chr17: 53,474,121-53,474,625 MMD
    nsv5424055mobile element insertion1nstd206human GRCh38 chr17: 55,393,985-55,394,036 , GRCh37.p13 chr17: 53,471,346-53,471,397 MMD
    nsv5153506mobile element insertion1nstd203human GRCh38 chr17: 55,393,970-55,393,985 , GRCh37.p13 chr17: 53,471,331-53,471,346 MMD
    nsv5026560copy number variation1nstd200human GRCh38 chr17: 55,409,949-55,412,025 , GRCh37.p13 chr17: 53,487,310-53,489,386 MMD
    nsv5026559copy number variation1nstd200human GRCh38 chr17: 55,399,324-55,409,668 , GRCh37.p13 chr17: 53,476,685-53,487,029 MMD
    nsv4571000sequence alteration1nstd166human GRCh37.p13 chr17: 53,490,674-53,492,255 , GRCh38.p12 chr17: 55,413,313-55,414,894 MMD
    nsv4566133mobile element insertion1nstd166human GRCh37.p13 chr17: 53,470,007-53,470,007 , GRCh38.p12 chr17: 55,392,646-55,392,646 MMD
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