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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098840copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,756,763-37,112,145 , GRCh38.p12 chr5: 36,756,661-37,112,043 NIPBL, CPLANE1, 3 more genes
    nsv7097143copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,953,718-37,371,079 , GRCh38.p12 chr5: 36,953,616-37,370,977 NUP155, OFD1P17, 7 more genes
    nsv7097142copy number variation1nstd102humanUncertain significance GRCh37 chr5: 36,953,718-37,324,229 , GRCh38.p12 chr5: 36,953,616-37,324,127 NIPBL, OFD1P17, 6 more genes
    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
    nsv7050297inversion1nstd229human GRCh38 chr5: 36,828,847-37,157,005 , GRCh37.p13 chr5: 36,828,949-37,157,107 CPLANE1, NIPBL, 4 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
    nsv6774369copy number variation1nstd229human GRCh38 chr5: 36,885,231-37,337,542 , GRCh37.p13 chr5: 36,885,333-37,337,644 RNU7-75P, NIPBL, 8 more genes
    nsv6771367copy number variation1nstd229human GRCh38 chr5: 37,054,281-37,285,916 , GRCh37.p13 chr5: 37,054,383-37,286,018 CPLANE1-AS1, RPS4XP6, 5 more genes
    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
    nsv6764962copy number variation1nstd229human GRCh38 chr5: 37,059,503-37,652,910 , GRCh37.p13 chr5: 37,059,605-37,653,012 KCTD9P5, OFD1P17, 10 more genes
    nsv6762045copy number variation1nstd229human GRCh38 chr5: 37,002,501-37,157,000 , GRCh37.p13 chr5: 37,002,603-37,157,102 RBISP2, RPS4XP6, 2 more genes
    nsv6761524copy number variation1nstd229human GRCh38 chr5: 37,051,252-37,139,157 , GRCh37.p13 chr5: 37,051,354-37,139,259 CPLANE1, RBISP2, 2 more genes
    nsv6760495copy number variation1nstd229human GRCh38 chr5: 36,904,559-37,604,845 , GRCh37.p13 chr5: 36,904,661-37,604,947 OFD1P17, NIPBL, 9 more genes
    nsv6636978copy number variation1nstd102humanUncertain significance GRCh37 chr5: 37,044,026-37,374,124 , GRCh38.p12 chr5: 37,043,924-37,374,022 CPLANE1, RN7SL37P, 7 more genes
    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
    nsv6386853copy number variation1nstd223human GRCh38 chr5: 36,885,231-37,337,537 , GRCh37.p13 chr5: 36,885,333-37,337,639 CPLANE1, RNU7-75P, 8 more genes
    nsv6378293copy number variation1nstd223human GRCh38 chr5: 37,047,457-37,384,377 , GRCh37.p13 chr5: 37,047,559-37,384,479 RPS4XP6, NUP155, 8 more genes
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
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