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Items: 1 to 20 of 955

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147805copy number variation1nstd232human GRCh37.p13 chr16: 89,408,395-89,408,484 , GRCh38.p12 chr16: 89,341,987-89,342,076 ANKRD11
    nsv7146107copy number variation1nstd232human GRCh37.p13 chr16: 89,464,749-89,464,870 , GRCh38.p12 chr16: 89,398,341-89,398,462 ANKRD11
    nsv7140094copy number variation1nstd232human GRCh37.p13 chr16: 89,389,953-89,390,012 , GRCh38.p12 chr16: 89,323,545-89,323,604 ANKRD11, LOC100287036
    nsv7137789copy number variation1nstd232human GRCh37.p13 chr16: 89,356,746-89,356,904 , GRCh38.p12 chr16: 89,290,338-89,290,496 ANKRD11
    nsv7099295copy number variation1nstd231human GRCh37 chr16: 89,399,270-89,505,521 , GRCh38.p12 chr16: 89,332,862-89,439,113 ANKRD11, LOC101927817
    nsv7099294copy number variation1nstd231human GRCh37 chr16: 89,394,004-89,490,401 , GRCh38.p12 chr16: 89,327,596-89,423,993 ANKRD11
    nsv7095116copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,556,969 , GRCh38.p12 chr16: 89,490,245-89,490,561 LOC101930112, LOC101927863, 1 more genes
    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
    nsv7095062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,851,392 , GRCh38.p12 chr16: 89,490,245-89,784,984 SNORD68, CHMP1A, 15 more genes
    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
    nsv7094939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,371,594-89,730,828 , GRCh38.p12 chr16: 89,305,186-89,664,420 LOC101930112, LOC101927863, 12 more genes
    nsv7094704copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,334,886-89,723,996 , GRCh38.p12 chr16: 89,268,478-89,657,588 LOC101930112, LOC101927863, 13 more genes
    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
    nsv7094616copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,484,692-89,484,776 , GRCh38.p12 chr16: 89,418,284-89,418,368 ANKRD11
    nsv7094615copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,334,886-89,371,772 , GRCh38.p12 chr16: 89,268,478-89,305,364 LOC105371414, ANKRD11
    nsv7076955inversion1nstd229human GRCh38 chr16: 89,393,444-89,441,453 , GRCh37.p13 chr16: 89,459,852-89,507,861 ANKRD11, RNU6-430P, 1 more genes
    nsv7075900inversion1nstd229human GRCh38 chr16: 89,427,513-89,433,876 , GRCh37.p13 chr16: 89,493,921-89,500,284 ANKRD11, LOC101927817
    nsv7074759inversion1nstd229human GRCh38 chr16: 89,342,057-89,342,192 , GRCh37.p13 chr16: 89,408,465-89,408,600 ANKRD11
    nsv7067380inversion1nstd229human GRCh38 chr16: 89,364,733-89,364,768 , GRCh37.p13 chr16: 89,431,141-89,431,176 ANKRD11
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