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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7051344inversion1nstd229human GRCh38 chr5: 36,271,641-38,407,431 , GRCh37.p13 chr5: 36,271,743-38,407,533 OFD1P17, NIPBL-DT, 29 more genes
    nsv7046165inversion1nstd229human GRCh38 chr5: 36,256,892-38,407,123 , GRCh37.p13 chr5: 36,256,994-38,407,225 NIPBL-DT, LINC02117, 29 more genes
    nsv7044509inversion1nstd229human GRCh38 chr5: 36,271,640-38,419,066 , GRCh37.p13 chr5: 36,271,742-38,419,168 WDR70, LINC02119, 29 more genes
    nsv6776781copy number variation1nstd229human GRCh38 chr5: 36,298,158-36,300,497 , GRCh37.p13 chr5: 36,298,260-36,300,599 RANBP3L
    nsv6773182copy number variation1nstd229human GRCh38 chr5: 36,256,901-36,263,200 , GRCh37.p13 chr5: 36,257,003-36,263,302 RANBP3L
    nsv6772078copy number variation1nstd229human GRCh38 chr5: 36,250,401-36,255,800 , GRCh37.p13 chr5: 36,250,503-36,255,902 RANBP3L
    nsv6770994copy number variation1nstd229human GRCh38 chr5: 36,215,312-36,275,708 , GRCh37.p13 chr5: 36,215,414-36,275,810 NADK2, RANBP3L
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6768014copy number variation1nstd229human GRCh38 chr5: 36,263,166-36,269,799 , GRCh37.p13 chr5: 36,263,268-36,269,901 RANBP3L
    nsv6767166copy number variation1nstd229human GRCh38 chr5: 36,286,306-36,291,149 , GRCh37.p13 chr5: 36,286,408-36,291,251 RANBP3L
    nsv6764929copy number variation1nstd229human GRCh38 chr5: 36,244,701-36,248,200 , GRCh37.p13 chr5: 36,244,803-36,248,302 RANBP3L
    nsv6762217copy number variation1nstd229human GRCh38 chr5: 36,239,665-36,245,897 , GRCh37.p13 chr5: 36,239,767-36,245,999 NADK2, RANBP3L
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630401copy number variation1nstd224human GRCh37 chr5: 36,195,350-36,324,582 , GRCh38.p12 chr5: 36,195,248-36,324,480 NADK2, RANBP3L
    nsv6630343copy number variation1nstd224human GRCh37 chr5: 36,251,432-36,369,103 , GRCh38.p12 chr5: 36,251,330-36,369,001 RANBP3L
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6568078inversion1nstd223human GRCh38 chr5: 36,265,975-36,266,757 , GRCh37.p13 chr5: 36,266,077-36,266,859 RANBP3L
    nsv6384656copy number variation1nstd223human GRCh38 chr5: 36,244,000-36,246,018 , GRCh37.p13 chr5: 36,244,102-36,246,120 RANBP3L
    nsv6383482copy number variation1nstd223human GRCh38 chr5: 36,256,033-36,256,489 , GRCh37.p13 chr5: 36,256,135-36,256,591 RANBP3L
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