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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047284inversion1nstd229human GRCh38 chr5: 18,365,039-24,500,882 , GRCh37.p13 chr5: 18,365,148-24,500,991 LOC105374683, SNORA105A, 40 more genes
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7046828inversion1nstd229human GRCh38 chr5: 18,870,000-23,244,369 , GRCh37.p13 chr5: 18,870,109-23,244,478 LOC105374683, GUSBP1, 28 more genes
    nsv7045172inversion1nstd229human GRCh38 chr5: 18,376,939-24,500,874 , GRCh37.p13 chr5: 18,377,048-24,500,983 LOC102723561, LOC100420804, 40 more genes
    nsv6777395copy number variation1nstd229human GRCh38 chr5: 21,698,901-23,136,400 , GRCh37.p13 chr5: 21,699,010-23,136,509 GCNT1P2, LOC101929617, 9 more genes
    nsv6759139copy number variation1nstd229human GRCh38 chr5: 18,173,837-22,856,339 , GRCh37.p13 chr5: 18,173,946-22,856,448 CDH12, LOC105374685, 28 more genes
    nsv6758719copy number variation1nstd229human GRCh38 chr5: 18,040,306-26,567,940 , GRCh37.p13 chr5: 18,040,415-26,568,049 CDH12, LINC02899, 49 more genes
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6636480copy number variation1nstd102humanUncertain significance GRCh37 chr5: 22,130,874-22,556,566 , GRCh38.p12 chr5: 22,130,765-22,556,457 LOC105374682, PMCHL1, 1 more genes
    nsv6389432copy number variation1nstd223human GRCh38 chr5: 22,131,677-22,558,617 , GRCh37.p13 chr5: 22,131,786-22,558,726 PMCHL1, LOC105374682, 1 more genes
    nsv6384015copy number variation1nstd223human GRCh38 chr5: 22,143,701-22,145,100 , GRCh37.p13 chr5: 22,143,810-22,145,209 PMCHL1, CDH12
    nsv6377907copy number variation1nstd223human GRCh38 chr5: 22,144,001-22,146,400 , GRCh37.p13 chr5: 22,144,110-22,146,509 PMCHL1, CDH12
    nsv6376566copy number variation1nstd223human GRCh38 chr5: 22,145,601-22,147,400 , GRCh37.p13 chr5: 22,145,710-22,147,509 PMCHL1, CDH12
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6136143copy number variation1nstd213human GRCh37 chr5: 9,360,000-26,560,001 , GRCh38.p12 chr5: 9,359,888-26,559,892 FTH1P10, MYO10, 163 more genes
    nsv6136106copy number variation1nstd213human GRCh37 chr5: 21,430,000-22,730,001 , GRCh38.p12 chr5: 21,429,891-22,729,892 GCNT1P2, LOC105374685, 9 more genes
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