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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097119copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,117,614-138,287,593 , GRCh38.p12 chr5: 138,781,925-138,951,904 SIL1, CTNNA1, 1 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
    nsv7096754copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,145,717-138,269,778 , GRCh38.p12 chr5: 138,810,028-138,934,089 CTNNA1, LRRTM2
    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
    nsv7046428inversion1nstd229human GRCh38 chr5: 138,736,216-139,021,639 , GRCh37.p13 chr5: 138,071,905-138,357,328 CTNNA1-AS1, CTNNA1, 3 more genes
    nsv6793499copy number variation1nstd229human GRCh38 chr5: 138,867,988-138,869,666 , GRCh37.p13 chr5: 138,203,677-138,205,355 CTNNA1, LRRTM2
    nsv6783598copy number variation1nstd229human GRCh38 chr5: 138,865,972-138,869,781 , GRCh37.p13 chr5: 138,201,661-138,205,470 CTNNA1, LRRTM2
    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
    nsv6412072copy number variation1nstd223human GRCh38 chr5: 138,865,972-138,869,781 , GRCh37.p13 chr5: 138,201,661-138,205,470 LRRTM2, CTNNA1
    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
    nsv6312178copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,117,614-138,266,634 , GRCh38.p12 chr5: 138,781,925-138,930,945 LRRTM2, CTNNA1
    nsv6135631copy number variation1nstd213human GRCh37 chr5: 138,101,563-138,316,580 , GRCh38.p12 chr5: 138,765,874-138,980,891 CTNNA1, LRRTM2, 1 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
    nsv6135115copy number variation1nstd213human GRCh37 chr5: 137,330,000-138,340,001 , GRCh38.p12 chr5: 137,994,311-139,004,312 HSPA9, KIF20A, 27 more genes
    nsv5381513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,118,846-138,269,778 , GRCh38.p12 chr5: 138,783,157-138,934,089 LRRTM2, CTNNA1
    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
    nsv5381376copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,088,085-138,271,723 , GRCh38.p12 chr5: 138,752,396-138,936,034 CTNNA1, CTNNA1-AS1, 1 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
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