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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5472900copy number variation1nstd206human GRCh38 chr5: 134,505,190-134,505,453 , GRCh37.p13 chr5: 133,840,881-133,841,144 LINC01843
    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
    nsv4945094copy number variation1nstd200human GRCh38 chr5: 134,482,541-134,539,491 , GRCh37.p13 chr5: 133,818,232-133,875,181 , RN7SL541P, 3 more genes
    nsv4938685copy number variation1nstd200human GRCh38 chr5: 134,504,431-134,509,857 , GRCh37.p13 chr5: 133,840,122-133,845,548 LINC01843
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 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
    nsv4131692copy number variation1nstd166human GRCh37.p13 chr5: 133,769,523-133,940,562 , GRCh38.p12 chr5: 134,433,832-134,604,872 , JADE2, 6 more genes
    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
    nsv3924484copy number variation1nstd102humanPathogenic NCBI36 chr5: 132,894,824-134,211,267 , GRCh38 chr5: 133,531,234-134,847,678 , GRCh37 chr5: 132,866,925-134,183,368 C5orf24, UBE2B, 28 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
    nsv3919979copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626 FBXL21P, MIR5692C1, 92 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
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
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