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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077569inversion1nstd229human GRCh38 chr8: 72,847,163-78,693,142 , GRCh37.p13 chr8: 73,759,398-79,605,377 RDH10-AS1, PI15, 61 more genes
    nsv7072725inversion1nstd229human GRCh38 chr8: 73,250,658-74,373,186 , GRCh37.p13 chr8: 74,162,893-75,285,421 RPS20P21, C8orf89, 22 more genes
    nsv7064031inversion1nstd229human GRCh38 chr8: 72,138,738-75,988,244 , GRCh37.p13 chr8: 73,050,973-76,900,479 RNU6-1300P, RNU6-285P, 49 more genes
    nsv6858066copy number variation1nstd229human GRCh38 chr8: 73,912,974-74,271,181 , GRCh37.p13 chr8: 74,825,209-75,183,416 RPS3AP32, DSTNP3, 9 more genes
    nsv6850174copy number variation1nstd229human GRCh38 chr8: 73,867,372-74,551,526 , GRCh37.p13 chr8: 74,779,607-75,463,761 MIR5681A, JPH1, 14 more genes
    nsv6845648copy number variation1nstd229human GRCh38 chr8: 73,883,839-74,279,899 , GRCh37.p13 chr8: 74,796,074-75,192,134 LOC105375903, RNU6-1300P, 9 more genes
    nsv6637040copy number variation1nstd102humanUncertain significance GRCh37 chr8: 74,515,647-75,122,801 , GRCh38.p12 chr8: 73,603,412-74,210,566 STAU2, RN7SL760P, 13 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6575523inversion1nstd223human GRCh38 chr8: 72,881,788-80,095,071 , GRCh37.p13 chr8: 73,794,023-81,007,306 ZFHX4-AS1, LINC01111, 82 more genes
    nsv6420262copy number variation1nstd223human GRCh38 chr8: 73,867,372-74,551,522 , GRCh37.p13 chr8: 74,779,607-75,463,757 RNU6-1300P, LOC105375903, 14 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6312655copy number variation1nstd102humanPathogenic GRCh37 chr8: 74,890,971-74,903,809 , GRCh38.p12 chr8: 73,978,736-73,991,574 LY96, TMEM70, 2 more genes
    nsv6312654copy number variation2nstd102humanUncertain significance GRCh37 chr8: 74,888,517-75,276,602 , GRCh38.p12 chr8: 73,976,282-74,364,367 DSTNP3, JPH1, 8 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136596copy number variation1nstd213human GRCh37 chr8: 72,190,000-86,530,001 , GRCh38.p12 chr8: 71,277,765-85,617,772 ACTBP6, CA2, 173 more genes
    nsv6136071copy number variation1nstd213human GRCh37 chr8: 74,240,000-75,150,001 , GRCh38.p12 chr8: 73,327,765-74,237,766 ELOC, RPS3AP32, 17 more genes
    nsv5919342copy number variation1nstd209human GRCh38 chr8: 72,905,491-79,590,734 , GRCh37.p13 chr8: 73,817,726-80,502,969 , GYG1P1, 73 more genes
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv4682621copy number variation2nstd102humanUncertain significance GRCh37 chr8: 74,888,367-75,279,355 , GRCh38.p12 chr8: 73,976,132-74,367,120 TMEM70, JPH1, 8 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
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