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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930590copy number variation1nstd209human GRCh38 chr13: 27,450,760-27,450,866 , GRCh37.p13 chr13: 28,024,897-28,025,003 MTIF3
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5319647copy number variation1nstd204human GRCh38.p13 chr13: 27,401,280-27,501,044 , GRCh37.p13 chr13: 27,975,417-28,075,181 MTIF3, RNY1P1, 2 more genes
    nsv5278066copy number variation1nstd204human GRCh38.p13 chr13: 27,401,301-27,501,100 , GRCh37.p13 chr13: 27,975,438-28,075,237 MTIF3, RNU6-63P, 2 more genes
    nsv5004435copy number variation1nstd200human GRCh38 chr13: 27,401,290-27,501,035 , GRCh37.p13 chr13: 27,975,427-28,075,172 RNU6-63P, RNY1P1, 2 more genes
    nsv4835473copy number variation1nstd200human GRCh37 chr13: 27,975,427-28,075,172 , GRCh38.p12 chr13: 27,401,290-27,501,035 RNY1P1, RNU6-63P, 2 more genes
    nsv4729520copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 23,775,339-30,534,624 , GRCh38.p12 chr13: 23,201,200-29,960,487 PARP4, ATP12A, 136 more genes
    nsv4685760copy number variation1nstd102humanUncertain significance GRCh37 chr13: 27,868,211-28,115,389 , GRCh38.p12 chr13: 27,294,074-27,541,252 GTF3A, RNU6-70P, 4 more genes
    nsv4226419copy number variation1nstd166human GRCh37.p13 chr13: 28,010,910-28,012,685 , GRCh38.p12 chr13: 27,436,773-27,438,548 MTIF3
    nsv4222518copy number variation1nstd166human GRCh37.p13 chr13: 28,023,380-28,023,855 , GRCh38.p12 chr13: 27,449,243-27,449,718 MTIF3
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3922871copy number variation1nstd102humanLikely benign NCBI36 chr13: 26,774,782-26,968,687 , GRCh37 chr13: 27,876,782-28,070,687 , GRCh38 chr13: 27,302,645-27,496,550 RNU6-63P, RNU6-70P, 4 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921601copy number variation1nstd102humanLikely pathogenic NCBI36 chr13: 26,437,381-29,569,995 , GRCh37 chr13: 27,539,381-30,671,995 , GRCh38 chr13: 26,965,244-30,097,858 CDX2, FLT1, 58 more genes
    nsv3921223copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141 TRIM60P13, LINC00351, 1289 more genes
    nsv3920749copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191 DIAPH3-AS2, LOC105370216, 1281 more genes
    nsv3919574copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750 RNU6-77P, LINC00457, 1317 more genes
    nsv3917322copy number variation2nstd102humanPathogenic NCBI36 chr13: 19,309,535-114,110,750 , GRCh37 chr13: 20,411,535-115,085,141 , GRCh38 chr13: 19,837,395-114,327,173 RNY1P7, LINC01039, 1283 more genes
    nsv3916629copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173 TM9SF2, LOC107984564, 1330 more genes
    nsv3916116copy number variation1nstd102humanPathogenic NCBI36 chr13: 19,305,270-114,110,683 , GRCh38 chr13: 19,833,130-114,327,106 , GRCh37 chr13: 20,407,270-115,085,141 LOC105370263, RPS7P10, 1283 more genes
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