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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069370inversion1nstd229human GRCh38 chr8: 74,779,865-81,220,765 , GRCh37.p13 chr8: 75,692,100-82,133,000 THAP12P7, LOC105375905, 69 more genes
    nsv6854481copy number variation1nstd229human GRCh38 chr8: 80,486,401-80,488,000 , GRCh37.p13 chr8: 81,398,636-81,400,235 ZBTB10
    nsv6854412copy number variation1nstd229human GRCh38 chr8: 79,890,335-80,518,448 , GRCh37.p13 chr8: 80,802,570-81,430,683 TPD52, RN7SL41P, 12 more genes
    nsv6853215copy number variation1nstd229human GRCh38 chr8: 75,371,044-80,542,313 , GRCh37.p13 chr8: 76,283,279-81,454,548 PKIA, LINC02605, 50 more genes
    nsv6844226copy number variation1nstd229human GRCh38 chr8: 80,383,813-80,483,708 , GRCh37.p13 chr8: 81,296,048-81,395,943 ZBTB10, RNU6-1213P, 2 more genes
    nsv6636819copy number variation1nstd102humanUncertain significance GRCh37 chr8: 79,876,744-83,112,711 , GRCh38.p12 chr8: 78,964,509-82,200,476 SLC25A51P3, PMP2, 59 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 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
    nsv6557187inversion1nstd223human GRCh38 chr8: 80,512,515-80,513,293 , GRCh37.p13 chr8: 81,424,750-81,425,528 ZBTB10
    nsv6557078inversion1nstd223human GRCh38 chr8: 80,506,361-80,507,305 , GRCh37.p13 chr8: 81,418,596-81,419,540 ZBTB10
    nsv6431293copy number variation1nstd223human GRCh38 chr8: 80,524,536-80,525,254 , GRCh37.p13 chr8: 81,436,771-81,437,489 ZBTB10
    nsv6422044copy number variation1nstd223human GRCh38 chr8: 80,521,201-80,522,500 , GRCh37.p13 chr8: 81,433,436-81,434,735 ZBTB10
    nsv6416328copy number variation1nstd223human GRCh38 chr8: 80,493,341-80,719,587 , GRCh37.p13 chr8: 81,405,576-81,631,822 SLC25A51P3, OCIAD2P1, 7 more genes
    nsv6315163copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854 ZNF704, RN7SL107P, 137 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
    nsv6313579copy number variation1nstd102humanPathogenic GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479 LOC105375915, LOC105375918, 143 more genes
    nsv6137307copy number variation1nstd213human GRCh37 chr8: 81,080,000-81,470,001 , GRCh38.p12 chr8: 80,167,765-80,557,766 ZBTB10, RPS5P5, 10 more genes
    nsv6136697copy number variation1nstd213human GRCh37 chr8: 80,760,000-81,600,001 , GRCh38.p12 chr8: 79,847,765-80,687,766 SLC25A51P3, MIR5708, 21 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
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