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Items: 1 to 20 of 205

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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
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7062540inversion1nstd229human GRCh38 chr8: 126,857,766-129,574,185 , GRCh37.p13 chr8: 127,870,011-130,586,431 CASC21, POU5F1B, 28 more genes
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6849554copy number variation1nstd229human GRCh38 chr8: 129,231,263-129,235,005 , GRCh37.p13 chr8: 130,243,509-130,247,251 LINC00977
    nsv6839045copy number variation1nstd229human GRCh38 chr8: 129,214,805-129,214,963 , GRCh37.p13 chr8: 130,227,051-130,227,209 LINC00977
    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
    nsv6632250copy number variation1nstd224human GRCh37 chr8: 130,123,196-130,547,253 , GRCh38.p12 chr8: 129,110,950-129,535,007 MIR3686, RN7SKP206, 2 more genes
    nsv6435557copy number variation1nstd223human GRCh38 chr8: 129,221,601-129,222,700 , GRCh37.p13 chr8: 130,233,847-130,234,946 LINC00977
    nsv6434453copy number variation1nstd223human GRCh38 chr8: 129,232,701-129,235,800 , GRCh37.p13 chr8: 130,244,947-130,248,046 LINC00977
    nsv6425827copy number variation1nstd223human GRCh38 chr8: 129,232,610-129,233,092 , GRCh37.p13 chr8: 130,244,856-130,245,338 LINC00977
    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
    nsv6290242copy number variation1nstd102humanUncertain significance GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134 LINC02055, LOC101927798, 100 more genes
    nsv6137048copy number variation1nstd213human GRCh37 chr8: 128,200,000-131,040,001 , GRCh38.p12 chr8: 127,187,755-130,027,755 CYRIB, GSDMC, 29 more genes
    nsv6136319copy number variation1nstd213human GRCh37 chr8: 129,280,000-132,570,001 , GRCh38.p12 chr8: 128,267,754-131,557,754 CYRIB, GSDMC, 21 more genes
    nsv6136318copy number variation1nstd213human GRCh37 chr8: 128,550,000-134,990,001 , GRCh38.p12 chr8: 127,537,755-133,977,758 CCN4, PHF20L1, 67 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
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