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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7097891copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,515,613-126,379,127 , GRCh38.p12 chr8: 123,503,373-125,366,885 FER1L6-AS1, LOC112268031, 35 more genes
    nsv7065632inversion1nstd229human GRCh38 chr8: 124,740,246-125,017,267 , GRCh37.p13 chr8: 125,752,488-126,029,509 MIR4662A, MIR4662B, 8 more genes
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6851858copy number variation1nstd229human GRCh38 chr8: 124,810,518-125,324,458 , GRCh37.p13 chr8: 125,822,760-126,336,700 RN7SL329P, LOC105375742, 10 more genes
    nsv6840099copy number variation1nstd229human GRCh38 chr8: 124,930,235-124,941,960 , GRCh37.p13 chr8: 125,942,477-125,954,202 LOC105375742, LINC00964
    nsv6839565copy number variation1nstd229human GRCh38 chr8: 124,940,607-124,947,058 , GRCh37.p13 chr8: 125,952,849-125,959,300 LINC00964
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 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
    nsv6418904copy number variation1nstd223human GRCh38 chr8: 124,854,801-124,959,700 , GRCh37.p13 chr8: 125,867,043-125,971,942 LINC00964, MRS2P1, 2 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 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
    nsv6136313copy number variation1nstd213human GRCh37 chr8: 124,820,000-126,220,001 , GRCh38.p12 chr8: 123,807,760-125,207,759 NDUFB9, TRMT12, 28 more genes
    nsv6136309copy number variation1nstd213human GRCh37 chr8: 122,920,000-127,650,001 , GRCh38.p12 chr8: 121,907,761-126,637,756 TBC1D31, FAM91A1, 77 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135822copy number variation1nstd213human GRCh37 chr8: 124,520,000-127,320,001 , GRCh38.p12 chr8: 123,507,760-126,307,756 RNF139, LINC00964, 42 more genes
    nsv5487461copy number variation1nstd206human GRCh38 chr8: 124,854,856-124,959,719 , GRCh37.p13 chr8: 125,867,098-125,971,961 MRS2P1, LOC105375743, 2 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
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