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Items: 1 to 20 of 583

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7097188copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,798,247-195,803,970 , GRCh38.p12 chr3: 196,071,376-196,077,099 TFRC, RNU7-18P
    nsv7096708copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,778,813-195,803,970 , GRCh38.p12 chr3: 196,051,942-196,077,099 TFRC, RNU7-18P
    nsv7055836inversion1nstd229human GRCh38 chr3: 195,821,822-196,257,566 , GRCh37.p13 chr3: 195,548,693-195,984,437 LOC100133326, LOC100131360, 15 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
    nsv7053308inversion1nstd229human GRCh38 chr3: 196,043,208-196,228,860 , GRCh37.p13 chr3: 195,770,079-195,955,731 LINC00885, TFRC, 4 more genes
    nsv7044786inversion1nstd229human GRCh38 chr3: 195,846,642-196,219,548 , GRCh37.p13 chr3: 195,573,513-195,946,419 LOC100131360, LOC105374304, 13 more genes
    nsv7044486inversion1nstd229human GRCh38 chr3: 195,703,983-196,043,070 , GRCh37.p13 chr3: 195,430,854-195,769,941 SMBD1P, LOC107984010, 13 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
    nsv7041063inversion1nstd229human GRCh38 chr3: 196,060,815-196,246,273 , GRCh37.p13 chr3: 195,787,686-195,973,144 TFRC, RNU7-18P, 5 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6736557copy number variation1nstd229human GRCh38 chr3: 196,047,100-196,048,078 , GRCh37.p13 chr3: 195,773,971-195,774,949 TFRC
    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
    nsv6730580copy number variation1nstd229human GRCh38 chr3: 195,808,566-196,246,187 , GRCh37.p13 chr3: 195,535,437-195,973,058 LOC100133326, MUC4, 16 more genes
    nsv6729546copy number variation1nstd229human GRCh38 chr3: 196,060,801-196,075,600 , GRCh37.p13 chr3: 195,787,672-195,802,471 TFRC, RNU7-18P
    nsv6728237copy number variation1nstd229human GRCh38 chr3: 196,013,345-196,020,552 , GRCh37.p13 chr3: 195,740,216-195,747,423 TFRC
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