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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6796049copy number variation1nstd229human GRCh38 chr5: 140,340,155-140,396,212 , GRCh37.p13 chr5: 139,719,740-139,775,797 RNU4-14P, HBEGF, 1 more genes
    nsv6786198copy number variation1nstd229human GRCh38 chr5: 140,326,901-140,332,500 , GRCh37.p13 chr5: 139,706,486-139,712,085 HBEGF
    nsv6783600copy number variation1nstd229human GRCh38 chr5: 140,306,014-140,360,169 , GRCh37.p13 chr5: 139,685,599-139,739,754 HBEGF, SLC4A9
    nsv6407401copy number variation1nstd223human GRCh38 chr5: 140,339,301-140,944,600 , GRCh37.p13 chr5: 139,718,886-140,144,409 IK, RNU4-14P, 43 more genes
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6397080copy number variation1nstd223human GRCh38 chr5: 140,340,155-140,396,210 , GRCh37.p13 chr5: 139,719,740-139,775,795 HBEGF, SLC4A9, 1 more genes
    nsv6290261copy number variation1nstd102humanPathogenic GRCh37 chr5: 139,493,717-140,517,454 , GRCh38.p12 chr5: 140,114,132-141,137,872 PCDHA2, RPL36P11, 57 more genes
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6011327copy number variation1nstd212human GRCh38 chr5: 140,340,025-140,340,317 , GRCh37.p13 chr5: 139,719,610-139,719,902 HBEGF
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 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
    nsv4455072copy number variation1nstd102humanUncertain significance GRCh37 chr5: 139,447,779-140,047,037 , GRCh38.p12 chr5: 140,068,194-140,667,452 LOC112267855, RNU4-14P, 23 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
    nsv3924309copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065 FCHSD1, LOC105378208, 183 more genes
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