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Items: 1 to 20 of 359

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673007copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,709,737-89,220,635 , GRCh38.p12 chr16: 88,643,329-89,154,227 MIR4722, PIEZO1, 23 more genes
    nsv5601563copy number variation1nstd207human GRCh38 chr16: 88,741,723-88,741,902 , GRCh37.p13 chr16: 88,808,131-88,808,310 PIEZO1, LOC339059, 1 more genes
    nsv5516784copy number variation1nstd206human GRCh38 chr16: 88,746,102-88,896,171 , GRCh37.p13 chr16: 88,812,510-88,962,579 , 10 more genes
    nsv5515834copy number variation1nstd206human GRCh38 chr16: 88,745,703-88,745,762 , GRCh37.p13 chr16: 88,812,111-88,812,170 LOC339059, PIEZO1
    nsv5289947copy number variation1nstd204human GRCh38.p13 chr16: 88,668,401-89,192,400 , GRCh37.p13 chr16: 88,734,809-89,258,808 , RNF166, 26 more genes
    nsv5287779copy number variation1nstd204human GRCh38.p13 chr16: 88,301,301-89,068,700 , GRCh37.p13 chr16: 88,334,907-89,135,108 , ZFPM1-AS1, 33 more genes
    nsv5015048copy number variation1nstd200human GRCh38 chr16: 88,742,708-88,742,804 , GRCh37.p13 chr16: 88,809,116-88,809,212 PIEZO1, LOC339059
    nsv5013563copy number variation1nstd200human GRCh38 chr16: 88,746,102-88,896,171 , GRCh37.p13 chr16: 88,812,510-88,962,579 , CBFA2T3, 10 more genes
    nsv4864376copy number variation1nstd200human GRCh37 chr16: 88,812,510-88,962,579 , GRCh38.p12 chr16: 88,746,102-88,896,171 , CDT1, 10 more genes
    nsv4851015copy number variation1nstd200human GRCh37 chr16: 88,800,202-88,836,304 , GRCh38.p12 chr16: 88,733,794-88,769,896 LOC339059, PIEZO1, 1 more genes
    nsv4742347copy number variation1nstd199human GRCh38.p12 chr16: 88,741,682-88,741,861 , GRCh37 chr16: 88,808,090-88,808,269 PIEZO1, LOC339059, 1 more genes
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4630604copy number variation1nstd183human GRCh37 chr16: 88,770,621-88,909,788 , GRCh38.p12 chr16: 88,704,213-88,843,380 , MIR4722, 9 more genes
    nsv4630049copy number variation1nstd183human GRCh37 chr16: 88,811,922-88,812,128 , GRCh38.p12 chr16: 88,745,514-88,745,720 PIEZO1, LOC339059
    nsv4627388copy number variation1nstd183human GRCh37 chr16: 88,807,776-88,808,346 , GRCh38.p12 chr16: 88,741,368-88,741,938 PIEZO1, LOC339059, 1 more genes
    nsv4626010copy number variation2nstd183human GRCh37 chr16: 88,705,417-88,830,206 , GRCh38.p12 chr16: 88,639,009-88,763,798 PIEZO1, MIR4722, 9 more genes
    nsv4623864copy number variation1nstd183human GRCh37 chr16: 88,773,738-88,818,586 , GRCh38.p12 chr16: 88,707,330-88,752,178 PIEZO1, CTU2, 3 more genes
    nsv4457118copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,782,844-89,140,571 , GRCh38.p12 chr16: 88,716,436-89,074,163 LOC102724632, LOC107983950, 16 more genes
    nsv4456065copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807 LOC101927863, LINC00304, 45 more genes
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