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Items: 1 to 20 of 877

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146238insertion1nstd232human GRCh37.p13 chr16: 89,184,330-89,184,330 , GRCh38.p12 chr16: 89,117,922-89,117,922 ACSF3
    nsv7144864copy number variation1nstd232human GRCh37.p13 chr16: 89,226,781-89,226,872 , GRCh38.p12 chr16: 89,160,373-89,160,464 ACSF3, LINC00304
    nsv7139364insertion1nstd232human GRCh37.p13 chr16: 89,178,457-89,178,457 , GRCh38.p12 chr16: 89,112,049-89,112,049 ACSF3
    nsv7095115copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 89,167,109-89,178,321 , GRCh38.p12 chr16: 89,100,701-89,111,913 ACSF3
    nsv7095112copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,870,240-89,484,776 , GRCh38.p12 chr16: 88,803,832-89,418,368 LOC101927793, LOC105371409, 21 more genes
    nsv7095061copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,220,488-89,222,264 , GRCh38.p12 chr16: 89,154,080-89,155,856 ACSF3
    nsv7095060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,883,023 , GRCh38.p12 chr16: 89,100,682-89,816,615 VPS9D1, ZNF276, 26 more genes
    nsv7095059copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,187,341 , GRCh38.p12 chr16: 89,100,682-89,120,933 ACSF3
    nsv7095058copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,167,090-89,169,187 , GRCh38.p12 chr16: 89,100,682-89,102,779 ACSF3
    nsv7094703copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,357,611 , GRCh38.p12 chr16: 89,100,682-89,291,203 ACSF3, LINC00304, 5 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7094613copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,199,534-89,222,264 , GRCh38.p12 chr16: 89,133,126-89,155,856 ACSF3
    nsv7094612copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,178,490-89,222,264 , GRCh38.p12 chr16: 89,112,082-89,155,856 ACSF3
    nsv7094611copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,167,090-89,220,615 , GRCh38.p12 chr16: 89,100,682-89,154,207 ACSF3
    nsv7094552copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,180,896-89,220,497 , GRCh38.p12 chr16: 89,114,488-89,154,089 ACSF3
    nsv7076684inversion1nstd229human GRCh38 chr16: 88,596,668-89,175,422 , GRCh37.p13 chr16: 88,663,076-89,241,830 LOC102724632, MIR4722, 28 more genes
    nsv7068378inversion1nstd229human GRCh38 chr16: 89,049,823-89,182,423 , GRCh37.p13 chr16: 89,116,231-89,248,831 ACSF3, LOC105371411, 4 more genes
    nsv7068262inversion1nstd229human GRCh38 chr16: 89,109,180-89,110,776 , GRCh37.p13 chr16: 89,175,588-89,177,184 ACSF3
    nsv6996337copy number variation1nstd229human GRCh38 chr16: 89,106,803-89,144,371 , GRCh37.p13 chr16: 89,173,211-89,210,779 ACSF3
    nsv6996227copy number variation1nstd229human GRCh38 chr16: 89,139,149-89,170,471 , GRCh37.p13 chr16: 89,205,557-89,236,879 ACSF3, LINC00304, 2 more genes
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