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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075434inversion1nstd229human GRCh38 chr19: 20,528,960-23,693,763 , GRCh37.p13 chr19: 20,845,947-23,876,565 LOC105372339, RPL36AP51, 124 more genes
    nsv7074397inversion1nstd229human GRCh38 chr19: 19,957,886-23,247,321 , GRCh37.p13 chr19: 20,068,695-23,430,123 ZNF723, LOC105372331, 135 more genes
    nsv7074115inversion1nstd229human GRCh38 chr19: 20,007,352-23,247,328 , GRCh37.p13 chr19: 20,118,161-23,430,130 BNIP3P33, VN1R82P, 134 more genes
    nsv7067666inversion1nstd229human GRCh38 chr19: 19,858,996-21,559,283 , GRCh37.p13 chr19: 19,969,805-21,742,085 VN1R81P, RNA5SP469, 72 more genes
    nsv7063071inversion1nstd229human GRCh38 chr19: 20,915,055-20,996,010 , GRCh37.p13 chr19: 21,097,861-21,178,816 ZNF85, KRT18P40, 2 more genes
    nsv7062147inversion1nstd229human GRCh38 chr19: 20,604,314-21,866,919 , GRCh37.p13 chr19: 20,845,947-22,049,721 BNIP3P24, LOC400682, 48 more genes
    nsv7061383inversion1nstd229human GRCh38 chr19: 20,296,571-21,048,763 , GRCh37.p13 chr19: 20,845,947-21,231,569 ZNF826P, LOC100418993, 29 more genes
    nsv7014525copy number variation1nstd229human GRCh38 chr19: 20,909,191-20,961,127 , GRCh37.p13 chr19: 21,091,997-21,143,933 KRT18P40, ZNF85, 2 more genes
    nsv7012079copy number variation1nstd229human GRCh38 chr19: 20,927,935-20,928,292 , GRCh37.p13 chr19: 21,110,741-21,111,098 ZNF85
    nsv7010294copy number variation1nstd229human GRCh38 chr19: 20,933,837-20,948,133 , GRCh37.p13 chr19: 21,116,643-21,130,939 ZNF85
    nsv7008649copy number variation1nstd229human GRCh38 chr19: 20,534,495-21,589,618 , GRCh37.p13 chr19: 20,845,947-21,772,420 ZNF737, ZNF431, 41 more genes
    nsv7008236copy number variation1nstd229human GRCh38 chr19: 20,813,401-20,951,800 , GRCh37.p13 chr19: 20,996,207-21,134,606 LOC100418987, LOC100418990, 7 more genes
    nsv7007383copy number variation1nstd229human GRCh38 chr19: 20,916,919-20,940,229 , GRCh37.p13 chr19: 21,099,725-21,123,035 ZNF85
    nsv7006068copy number variation1nstd229human GRCh38 chr19: 20,938,801-21,198,200 , GRCh37.p13 chr19: 21,121,607-21,381,003 VN1R82P, KRT18P40, 9 more genes
    nsv7002408copy number variation1nstd229human GRCh38 chr19: 20,950,906-20,951,327 , GRCh37.p13 chr19: 21,133,712-21,134,133 ZNF85
    nsv7000075copy number variation1nstd229human GRCh38 chr19: 20,938,869-20,938,904 , GRCh37.p13 chr19: 21,121,675-21,121,710 ZNF85
    nsv6998694copy number variation1nstd229human GRCh38 chr19: 20,945,128-20,952,024 , GRCh37.p13 chr19: 21,127,934-21,134,830 ZNF85
    nsv6637997copy number variation1nstd102humanUncertain significance GRCh37 chr19: 20,258,982-21,235,052 , GRCh38.p12 chr19: 20,148,173-21,052,246 BNIP3P17, LOC105372318, 38 more genes
    nsv6624879copy number variation1nstd224human GRCh37 chr19: 21,087,524-21,168,754 , GRCh38.p12 chr19: 20,904,718-20,985,948 , GRCh38.p12 chr19|NW_003315962.1: 247,994-329,224 ZNF85, KRT18P40, 4 more genes
    nsv6624847copy number variation1nstd224human GRCh37 chr19: 20,955,898-21,117,803 , GRCh38.p12 chr19: 20,773,092-20,934,997 , GRCh38.p12 chr19|NW_003315962.1: 109,952-278,273 ZNF66, ZNF85, 9 more genes
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