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Items: 1 to 20 of 134

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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
    nsv6853310copy number variation1nstd229human GRCh38 chr8: 73,876,596-73,877,302 , GRCh37.p13 chr8: 74,788,831-74,789,537 UBE2W, LINC01617
    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
    nsv6847963copy number variation1nstd229human GRCh38 chr8: 73,839,301-73,903,600 , GRCh37.p13 chr8: 74,751,536-74,815,835 UBE2W, GYG1P1, 1 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
    nsv6419293copy number variation1nstd223human GRCh38 chr8: 73,873,901-73,881,000 , GRCh37.p13 chr8: 74,786,136-74,793,235 UBE2W, LINC01617
    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
    nsv6308415insertion1nstd186human GRCh37 chr8: 74,793,789-74,793,793 , GRCh38.p12 chr8: 73,881,554-73,881,558 LINC01617
    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
    nsv6062480insertion1nstd212human GRCh38 chr8: 73,880,587-73,880,587 , GRCh37.p13 chr8: 74,792,822-74,792,822 LINC01617
    nsv5919342copy number variation1nstd209human GRCh38 chr8: 72,905,491-79,590,734 , GRCh37.p13 chr8: 73,817,726-80,502,969 , GYG1P1, 73 more genes
    nsv5541828insertion1nstd206human GRCh38 chr8: 73,881,554-73,881,558 , GRCh37.p13 chr8: 74,793,789-74,793,793 LINC01617
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
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