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Items: 1 to 20 of 319

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887240copy number variation1nstd209human GRCh38 chr1: 27,441,579-27,443,495 , GRCh37.p13 chr1: 27,768,093-27,770,008 WASF2
    nsv5884347copy number variation1nstd209human GRCh38 chr1: 27,477,646-27,480,779 , GRCh37.p13 chr1: 27,804,157-27,807,290 WASF2
    nsv5874638copy number variation1nstd209human GRCh38 chr1: 27,477,601-27,477,929 , GRCh37.p13 chr1: 27,804,112-27,804,440 WASF2
    nsv5871678copy number variation1nstd209human GRCh38 chr1: 27,441,732-27,442,520 , GRCh37.p13 chr1: 27,768,246-27,769,035 WASF2
    nsv5829965copy number variation1nstd209human GRCh38 chr1: 27,478,245-27,480,097 , GRCh37.p13 chr1: 27,804,756-27,806,608 WASF2
    nsv5725227mobile element insertion1nstd211human GRCh38 chr1: 27,415,728-27,415,728 , GRCh37.p13 chr1: 27,742,222-27,742,222 WASF2
    nsv5715337mobile element insertion1nstd211human GRCh38 chr1: 27,462,465-27,462,465 , GRCh37.p13 chr1: 27,788,976-27,788,976 WASF2
    nsv5611366insertion1nstd207human GRCh38 chr1: 27,487,644-27,487,644 , GRCh37.p13 chr1: 27,814,155-27,814,155 WASF2
    nsv5571966copy number variation1nstd207human GRCh38 chr1: 27,489,364-27,489,452 , GRCh37.p13 chr1: 27,815,875-27,815,963 WASF2
    nsv5571217copy number variation1nstd207human GRCh38 chr1: 27,477,601-27,477,929 , GRCh37.p13 chr1: 27,804,112-27,804,440 WASF2
    nsv5560667sequence alteration1nstd206human GRCh38 chr1: 27,467,229-27,468,545 , GRCh37.p13 chr1: 27,793,740-27,795,056 WASF2
    nsv5560072mobile element insertion1nstd206human GRCh38 chr1: 27,415,744-27,415,779 , GRCh37.p13 chr1: 27,742,238-27,742,273 WASF2
    nsv5544240insertion1nstd206human GRCh38 chr1: 27,409,077-27,409,170 , GRCh37.p13 chr1: 27,735,571-27,735,664 WASF2
    nsv5538912insertion1nstd206human GRCh38 chr1: 27,468,540-27,468,540 , GRCh37.p13 chr1: 27,795,051-27,795,051 WASF2
    nsv5432417copy number variation1nstd206human GRCh38 chr1: 27,477,617-27,477,930 , GRCh37.p13 chr1: 27,804,128-27,804,441 WASF2
    nsv5429547copy number variation1nstd206human GRCh38 chr1: 27,306,072-28,001,379 , GRCh37.p13 chr1: 27,632,563-28,327,890 SMPDL3B, SCARNA1, 28 more genes
    nsv5428924copy number variation1nstd206human GRCh38 chr1: 27,441,760-27,442,622 , GRCh37.p13 chr1: 27,768,275-27,769,137 WASF2
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5427415copy number variation1nstd206human GRCh38 chr1: 27,445,167-27,449,042 , GRCh37.p13 chr1: 27,771,680-27,775,554 WASF2
    nsv5426176copy number variation1nstd206human GRCh38 chr1: 27,471,062-27,477,617 , GRCh37.p13 chr1: 27,797,573-27,804,128 WASF2
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