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Items: 1 to 20 of 1983

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3557850mobile element insertion1nstd152human GRCh38 (hg38) chr9: 116,840,528-116,840,529 , GRCh37.p13 chr9: 119,602,807-119,602,808 ASTN2, LOC105376239
    nsv3557145insertion1nstd152human GRCh38 (hg38) chr9: 117,016,701-117,016,702 , GRCh37.p13 chr9: 119,778,980-119,778,981 ASTN2
    nsv3557139insertion1nstd152human GRCh38 (hg38) chr9: 116,840,525-116,840,526 , GRCh37.p13 chr9: 119,602,804-119,602,805 ASTN2, LOC105376239
    nsv3557116insertion1nstd152human GRCh38 (hg38) chr9: 117,016,713-117,016,714 , GRCh37.p13 chr9: 119,778,992-119,778,993 ASTN2
    nsv3555966insertion3nstd152human GRCh38 (hg38) chr9: 116,936,098-116,936,099 , GRCh37.p13 chr9: 119,698,377-119,698,378 ASTN2
    nsv3547760insertion1nstd152human GRCh38 (hg38) chr9: 116,840,559-116,840,560 , GRCh37.p13 chr9: 119,602,838-119,602,839 ASTN2, LOC105376239
    nsv3547003insertion1nstd152human GRCh38 (hg38) chr9: 116,840,551-116,840,552 , GRCh37.p13 chr9: 119,602,830-119,602,831 ASTN2, LOC105376239
    nsv3546534insertion1nstd152human GRCh38 (hg38) chr9: 117,060,510-117,060,511 , GRCh37.p13 chr9: 119,822,789-119,822,790 ASTN2
    nsv3528006copy number variation1nstd152human GRCh38 (hg38) chr9: 117,282,608-117,282,936 , GRCh37.p13 chr9: 120,044,887-120,045,215 ASTN2
    nsv3520015mobile element deletion5nstd152human GRCh38 (hg38) chr9: 116,439,185-116,439,500 , GRCh37.p13 chr9: 119,201,464-119,201,779 ASTN2
    nsv3418081mobile element deletion5nstd162human GRCh38 (hg38) chr9: 116,439,187-116,439,500 , GRCh37.p13 chr9: 119,201,466-119,201,779 ASTN2
    nsv3416725mobile element deletion12nstd162human GRCh38 (hg38) chr9: 116,714,786-116,715,119 , GRCh37.p13 chr9: 119,477,065-119,477,398 ASTN2
    nsv3409819insertion1nstd162human GRCh38 (hg38) chr9: 117,058,382-117,058,382 , GRCh37.p13 chr9: 119,820,661-119,820,661 ASTN2
    nsv3409803copy number variation1nstd162human GRCh38 (hg38) chr9: 117,127,653-117,127,703 , GRCh37.p13 chr9: 119,889,932-119,889,982 ASTN2
    nsv3406141insertion14nstd162human GRCh38 (hg38) chr9: 116,840,554-116,840,554 , GRCh37.p13 chr9: 119,602,833-119,602,833 ASTN2, LOC105376239
    nsv3399971insertion14nstd162human GRCh38 (hg38) chr9: 116,936,096-116,936,096 , GRCh37.p13 chr9: 119,698,375-119,698,375 ASTN2
    nsv3399642insertion7nstd162human GRCh38 (hg38) chr9: 117,016,700-117,016,700 , GRCh37.p13 chr9: 119,778,979-119,778,979 ASTN2
    nsv3245782insertion1nstd152human GRCh38 (hg38) chr9: 116,929,502-116,955,016 , GRCh37.p13 chr9: 119,691,781-119,717,295 ASTN2
    nsv3209606complex substitution1nstd152human GRCh38 (hg38) chr9: 117,351,745-117,351,808 , GRCh37.p13 chr9: 120,114,024-120,114,087 ASTN2
    nsv3195448complex substitution1nstd152human GRCh38 (hg38) chr9: 116,722,012-116,722,206 , GRCh37.p13 chr9: 119,484,291-119,484,485 ASTN2
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