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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097024copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,266,142-138,861,289 , GRCh38.p12 chr5: 138,930,453-139,481,704 SLC23A1, RNU5B-4P, 20 more genes
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    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
    nsv6796944copy number variation1nstd229human GRCh38 chr5: 139,310,340-139,400,844 , GRCh37.p13 chr5: 138,646,029-138,736,533 PROB1, PAIP2, 5 more genes
    nsv6788548copy number variation1nstd229human GRCh38 chr5: 139,383,598-139,392,308 , GRCh37.p13 chr5: 138,719,287-138,727,997 MZB1, SLC23A1, 1 more genes
    nsv6636861copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,893,096-138,868,605 , GRCh38.p12 chr5: 138,557,407-139,489,020 HSPA9, ECSCR, 27 more genes
    nsv6630305copy number variation1nstd224human GRCh37 chr5: 138,652,744-138,764,329 , GRCh38.p12 chr5: 139,317,055-139,428,640 MATR3, SLC23A1, 6 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
    nsv6291250copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,386,858-138,935,115 , GRCh38.p12 chr5: 139,051,169-139,555,530 STING1, SPATA24, 18 more genes
    nsv6291016copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,675,227-139,314,012 , GRCh38.p12 chr5: 139,339,538-139,934,427 PROB1, H3P25, 19 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
    nsv6135116copy number variation1nstd213human GRCh37 chr5: 138,320,000-138,890,001 , GRCh38.p12 chr5: 138,984,311-139,510,416 MATR3, SLC23A1, 20 more genes
    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
    nsv5221325copy number variation1nstd204human GRCh38.p13 chr5: 139,385,486-139,391,885 , GRCh37.p13 chr5: 138,721,175-138,727,574 MZB1, PROB1
    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
    nsv4769371copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 137,754,277-138,994,590 , GRCh38.p12 chr5: 138,418,588-139,615,005 CTNNA1, EGR1, 36 more genes
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