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Items: 1 to 20 of 613

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139210insertion1nstd232human GRCh37.p13 chr3: 196,089,558-196,089,558 , GRCh38.p12 chr3: 196,362,687-196,362,687 UBXN7
    nsv7098929copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334 LINC01063, RNF168, 52 more genes
    nsv7098781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,591,052-197,682,644 , GRCh38.p12 chr3: 195,864,181-197,955,773 ZDHHC19, DLG1, 68 more genes
    nsv7055557inversion1nstd229human GRCh38 chr3: 195,655,301-197,630,693 , GRCh37.p13 chr3: 195,382,172-197,357,564 MIR570HG, RN7SL434P, 66 more genes
    nsv7053852inversion1nstd229human GRCh38 chr3: 195,653,753-197,300,599 , GRCh37.p13 chr3: 195,380,624-197,027,470 NCBP2-AS1, SMCO1, 59 more genes
    nsv7053446inversion1nstd229human GRCh38 chr3: 195,340,377-197,478,980 , GRCh37.p13 chr3: 195,061,106-197,205,851 CEP19, ACAP2, 73 more genes
    nsv7050481inversion1nstd229human GRCh38 chr3: 196,292,084-196,493,779 , GRCh37.p13 chr3: 196,018,955-196,220,650 RNF168, TM4SF19-AS1, 10 more genes
    nsv7044295inversion1nstd229human GRCh38 chr3: 195,547,271-197,153,236 , GRCh37.p13 chr3: 195,274,089-196,880,107 SDHAP1, NCBP2AS2, 64 more genes
    nsv7044261inversion1nstd229human GRCh38 chr3: 195,438,610-197,225,061 , GRCh37.p13 chr3: 195,159,339-196,951,932 MUC4, RPL24P6, 67 more genes
    nsv6737421copy number variation1nstd229human GRCh38 chr3: 196,416,401-196,422,300 , GRCh37.p13 chr3: 196,143,272-196,149,171 UBXN7
    nsv6736336copy number variation1nstd229human GRCh38 chr3: 196,344,601-196,372,300 , GRCh37.p13 chr3: 196,071,472-196,099,171 UBXN7
    nsv6734915copy number variation1nstd229human GRCh38 chr3: 196,396,227-196,398,323 , GRCh37.p13 chr3: 196,123,098-196,125,194 UBXN7, RN7SL738P, 1 more genes
    nsv6733823copy number variation1nstd229human GRCh38 chr3: 196,423,359-196,427,994 , GRCh37.p13 chr3: 196,150,230-196,154,865 UBXN7
    nsv6733396copy number variation1nstd229human GRCh38 chr3: 196,054,229-196,418,828 , GRCh37.p13 chr3: 195,781,100-196,145,699 TM4SF19-DYNLT2B, RNU6-910P, 15 more genes
    nsv6732493copy number variation1nstd229human GRCh38 chr3: 196,396,070-196,396,295 , GRCh37.p13 chr3: 196,122,941-196,123,166 UBXN7, RN7SL434P
    nsv6729521copy number variation1nstd229human GRCh38 chr3: 196,438,008-196,443,631 , GRCh37.p13 chr3: 196,164,879-196,170,502 UBXN7
    nsv6729373copy number variation1nstd229human GRCh38 chr3: 196,357,971-196,358,021 , GRCh37.p13 chr3: 196,084,842-196,084,892 UBXN7
    nsv6728901copy number variation1nstd229human GRCh38 chr3: 196,423,436-196,432,179 , GRCh37.p13 chr3: 196,150,307-196,159,050 UBXN7, UBXN7-AS1
    nsv6728821copy number variation1nstd229human GRCh38 chr3: 196,202,777-196,997,902 , GRCh37.p13 chr3: 195,929,648-196,724,773 DYNLT2B, RN7SL434P, 35 more genes
    nsv6727107copy number variation1nstd229human GRCh38 chr3: 196,434,027-196,438,894 , GRCh37.p13 chr3: 196,160,898-196,165,765 UBXN7
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