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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv3900710copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,069,932-36,887,326 , GRCh38.p12 chr18: 22,489,969-39,307,362 CABLES1, PA2G4P3, 174 more genes
    nsv3912224copy number variation1nstd102humanPathogenic NCBI36 chr18: 27,945,491-39,904,182 , GRCh38 chr18: 32,111,530-44,070,219 , GRCh37 chr18: 29,691,493-41,650,184 SYT4, MIR4318, 94 more genes
    nsv4676233copy number variation1nstd102humanPathogenic GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790 DHFRP1, CLUHP6, 116 more genes
    nsv3912888copy number variation1nstd102humanPathogenic GRCh37 chr18: 27,024,475-37,983,616 , NCBI36 chr18: 25,278,473-36,237,614 , GRCh38 chr18: 29,444,510-40,403,652 KLHL14, ZNF271P, 107 more genes
    nsv3893439copy number variation1nstd102humanPathogenic GRCh37 chr8: 49,822,483-58,822,602 , GRCh38.p12 chr8: 48,909,924-57,910,043 MOS, SEPTIN10P1, 110 more genes
    nsv3911944copy number variation1nstd102humanPathogenic GRCh37 chr8: 54,237,949-62,775,577 , GRCh38 chr8: 53,325,389-61,863,018 , NCBI36 chr8: 54,400,502-62,938,131 MOS, SOX17, 119 more genes
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 MOS, LOC105375849, 103 more genes
    nsv3920302copy number variation1nstd102humanPathogenic NCBI36 chr18: 29,881,080-37,228,316 , GRCh38 chr18: 34,047,118-41,394,354 , GRCh37 chr18: 31,627,082-38,974,318 FHOD3, MIR3975, 61 more genes
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 MOS, NUDT15P1, 83 more genes
    nsv3897721copy number variation1nstd102humanPathogenic GRCh37 chr18: 29,711,972-35,866,193 , GRCh38.p12 chr18: 32,132,009-38,286,229 LOC105372073, CLUHP6, 56 more genes
    nsv3919070copy number variation1nstd102humanPathogenic NCBI36 chr8: 54,569,654-58,566,126 , GRCh37.p13 chr8: 54,407,101-58,403,572 , GRCh38.p12 chr8: 53,494,541-57,491,013 MOS, BPNT2, 73 more genes
    nsv3919101copy number variation1nstd102humanPathogenic GRCh38 chr8: 55,423,413-58,836,753 , NCBI36 chr8: 56,498,527-59,911,866 , GRCh37 chr8: 56,335,973-59,749,312 MOS, RPL37P6, 59 more genes
    nsv4350805copy number variation1nstd102humanPathogenic GRCh37 chr18: 33,554,981-36,939,357 , GRCh38.p12 chr18: 35,975,018-39,359,393 LOC101927879, LOC105372076, 28 more genes
    nsv3912773copy number variation1nstd102humanPathogenic GRCh37 chr8: 55,677,510-57,697,858 , NCBI36 chr8: 55,840,064-57,860,412 , GRCh38 chr8: 54,764,950-56,785,299 MOS, PSMC6P1, 36 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 MOS, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 MOS, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 MOS, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 MOS, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 MOS, SPAG1, 2105 more genes
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