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Items: 1 to 20 of 99

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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
    nsv6796360copy number variation1nstd229human GRCh38 chr5: 139,298,314-139,314,456 , GRCh37.p13 chr5: 138,634,003-138,650,145 RNA5SP195, MATR3
    nsv6780567copy number variation1nstd229human GRCh38 chr5: 139,264,264-139,309,626 , GRCh37.p13 chr5: 138,599,953-138,645,315 MATR3, SNHG4, 3 more genes
    nsv6778440copy number variation1nstd229human GRCh38 chr5: 139,104,141-139,300,722 , GRCh37.p13 chr5: 138,439,830-138,636,411 SNHG4, SNORA74A, 5 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
    nsv6562146inversion1nstd223human GRCh38 chr5: 139,300,095-139,300,825 , GRCh37.p13 chr5: 138,635,784-138,636,514 MATR3, RNA5SP195
    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
    nsv6311751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,608,441-138,668,366 , GRCh38.p12 chr5: 139,272,752-139,332,677 MATR3, SNORA74A, 4 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
    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
    nsv5718799mobile element insertion1nstd211human GRCh38 chr5: 139,298,679-139,298,679 , GRCh37.p13 chr5: 138,634,368-138,634,368 RNA5SP195, MATR3
    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
    nsv4945138copy number variation1nstd200human GRCh38 chr5: 139,264,188-139,309,695 , GRCh37.p13 chr5: 138,599,877-138,645,384 MATR3, RNA5SP195, 3 more genes
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