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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147897copy number variation1nstd232human GRCh37.p13 chr5: 149,755,890-149,755,981 , GRCh38.p12 chr5: 150,376,327-150,376,418 TCOF1
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6796085copy number variation1nstd229human GRCh38 chr5: 150,376,027-150,379,345 , GRCh37.p13 chr5: 149,755,590-149,758,908 TCOF1
    nsv6793649copy number variation1nstd229human GRCh38 chr5: 150,391,197-150,391,756 , GRCh37.p13 chr5: 149,770,760-149,771,319 TCOF1
    nsv6791983copy number variation1nstd229human GRCh38 chr5: 150,366,641-150,366,968 , GRCh37.p13 chr5: 149,746,204-149,746,531 TCOF1
    nsv6785278copy number variation1nstd229human GRCh38 chr5: 150,381,110-150,383,693 , GRCh37.p13 chr5: 149,760,673-149,763,256 TCOF1
    nsv6779186copy number variation1nstd229human GRCh38 chr5: 150,232,549-150,518,402 , GRCh37.p13 chr5: 149,612,112-149,897,964 RPS14, NDST1, 7 more genes
    nsv6630116copy number variation1nstd224human GRCh37 chr5: 149,755,421-149,810,153 , GRCh38.p12 chr5: 150,375,858-150,430,590 TCOF1, CD74
    nsv6414572copy number variation1nstd223human GRCh38 chr5: 150,374,196-150,438,419 , GRCh37.p13 chr5: 149,753,759-149,817,982 CD74, TCOF1
    nsv6410124copy number variation1nstd223human GRCh38 chr5: 150,381,110-150,383,690 , GRCh37.p13 chr5: 149,760,673-149,763,253 TCOF1
    nsv6406498copy number variation1nstd223human GRCh38 chr5: 150,379,875-150,381,923 , GRCh37.p13 chr5: 149,759,438-149,761,486 TCOF1
    nsv6406097copy number variation1nstd223human GRCh38 chr5: 150,394,901-150,395,600 , GRCh37.p13 chr5: 149,774,464-149,775,163 TCOF1
    nsv6401881copy number variation1nstd223human GRCh38 chr5: 150,366,628-150,366,954 , GRCh37.p13 chr5: 149,746,191-149,746,517 TCOF1
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv6007886copy number variation1nstd212human GRCh38 chr5: 150,366,628-150,366,954 , GRCh37.p13 chr5: 149,746,191-149,746,517 TCOF1
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