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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 TCF7, MEGF10, 2080 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 TCF7, TXNDC15, 962 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 TCF7, LINC01023, 783 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 TCF7, MIR1289-2, 138 more genes
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 TCF7, CSF2, 99 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TCF7, TGFBI, 110 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 TCF7, FBXL21P, 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 TCF7, SLC25A48-AS1, 96 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 TCF7, MTND5P11, 60 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 TCF7, C5orf24, 28 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 TCF7, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 TCF7, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 TCF7, SPEF2, 2490 more genes
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 TCF7, PJA2, 1228 more genes
    nsv3878636copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902 TCF7, LOC100288484, 551 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 TCF7, HNRNPA3P7, 514 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 TCF7, UQCRQ, 489 more genes
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 TCF7, ACTBP4, 157 more genes
    nsv3884275copy number variation1nstd102humanLikely benign GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409 TCF7, LOC107986368, 1258 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 TCF7, RNU1-150P, 1757 more genes
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