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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893039copy number variation1nstd209human GRCh38 chr5: 132,864,618-132,865,161 , GRCh37.p13 chr5: 132,200,310-132,200,853 UQCRQ, GDF9
    nsv5471660copy number variation1nstd206human GRCh38 chr5: 132,860,247-132,915,198 , GRCh37.p13 chr5: 132,195,939-132,250,890 GDF9, UQCRQ, 2 more genes
    nsv5461304copy number variation1nstd206human GRCh38 chr5: 132,864,618-132,865,164 , GRCh37.p13 chr5: 132,200,310-132,200,856 GDF9, UQCRQ
    nsv5362511translocation1nstd200human GRCh38 chr5: 132,864,618-132,864,618 , GRCh38 chr5: 132,865,164-132,865,164 , GRCh37.p13 chr5: 132,200,310-132,200,310 , GRCh37.p13 chr5: 132,200,856-132,200,856 UQCRQ, GDF9
    nsv5319150copy number variation1nstd204human GRCh38.p13 chr5: 132,864,616-132,865,165 , GRCh37.p13 chr5: 132,200,308-132,200,857 GDF9, UQCRQ
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4120176copy number variation1nstd166human GRCh37.p13 chr5: 132,200,310-132,200,856 , GRCh38.p12 chr5: 132,864,618-132,865,164 UQCRQ, GDF9
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
    nsv3923830copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,151,895-134,718,848 , GRCh38 chr5: 132,816,203-135,383,158 , NCBI36 chr5: 132,179,794-134,746,747 MTND5P11, TCF7, 60 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3920627copy number variation1nstd102humanPathogenic NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694 MIR1289-2, DCANP1, 138 more genes
    nsv3916850copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,962,196-135,150,743 , NCBI36 chr5: 130,990,095-135,178,642 , GRCh38 chr5: 131,626,503-135,815,054 SLC25A48-AS1, CTB-3M24.3, 96 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 UQCRQ, SNHG4, 489 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 more genes
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