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Items: 1 to 20 of 490

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138853insertion1nstd232human GRCh37.p13 chr6: 112,562,337-112,562,337 , GRCh38.p12 chr6: 112,241,136-112,241,136 LAMA4, LAMA4-AS1
    nsv7097566copy number variation1nstd102humanUncertain significance GRCh37 chr6: 112,508,632-112,508,823 , GRCh38.p12 chr6: 112,187,430-112,187,621 LAMA4
    nsv7053450inversion1nstd229human GRCh38 chr6: 112,228,366-112,286,553 , GRCh37.p13 chr6|NW_003871062.1: 225,887-262,912 , GRCh37.p13 chr6: 112,549,567-112,586,593 LAMA4, LOC107986632, 1 more genes
    nsv7049004inversion1nstd229human GRCh38 chr6: 112,119,798-112,119,820 , GRCh37.p13 chr6: 112,441,001-112,441,023 , GRCh37.p13 chr6|NW_003871062.1: 117,320-117,342 LAMA4, LOC107986633
    nsv7048821inversion1nstd229human GRCh38 chr6: 112,221,453-112,351,413 , GRCh37.p13 chr6: 112,586,594-112,672,615 LAMA4, LAMA4-AS1, 3 more genes
    nsv7047011inversion1nstd229human GRCh38 chr6: 112,212,900-112,221,951 , GRCh37.p13 chr6|NW_003871062.1: 210,421-219,472 , GRCh37.p13 chr6: 112,534,101-112,543,152 LAMA4
    nsv7046333inversion1nstd229human GRCh38 chr6: 112,252,766-112,256,689 , GRCh37.p13 chr6|NW_003871062.1: 250,287-254,210 , GRCh37.p13 chr6: 112,573,968-112,577,891 LAMA4, LAMA4-AS1
    nsv7040236inversion1nstd229human GRCh38 chr6: 111,756,087-112,191,364 , GRCh37.p13 chr6: 112,077,290-112,323,681 TUBE1, FYN, 7 more genes
    nsv7040174inversion1nstd229human GRCh38 chr6: 112,249,822-112,256,984 , GRCh37.p13 chr6|NW_003871062.1: 247,343-254,505 , GRCh37.p13 chr6: 112,571,024-112,578,186 LAMA4-AS1, LAMA4
    nsv7038953inversion1nstd229human GRCh38 chr6: 112,194,566-112,197,272 , GRCh37.p13 chr6|NW_003871062.1: 192,087-194,793 , GRCh37.p13 chr6: 112,515,768-112,518,474 LAMA4, RNU6-1226P
    nsv7038475inversion1nstd229human GRCh38 chr6: 112,146,785-112,146,798 , GRCh37.p13 chr6|NW_003871062.1: 144,306-144,319 , GRCh37.p13 chr6: 112,467,987-112,468,000 LOC107986633, LAMA4
    nsv6818040copy number variation1nstd229human GRCh38 chr6: 112,252,079-112,252,295 , GRCh37.p13 chr6: 112,573,281-112,573,497 , GRCh37.p13 chr6|NW_003871062.1: 249,600-249,816 LAMA4, LAMA4-AS1
    nsv6817349copy number variation1nstd229human GRCh38 chr6: 112,176,156-112,176,211 , GRCh37.p13 chr6: 112,497,358-112,497,413 , GRCh37.p13 chr6|NW_003871062.1: 173,677-173,732 LAMA4
    nsv6816302copy number variation1nstd229human GRCh38 chr6: 112,234,077-112,251,232 , GRCh37.p13 chr6|NW_003871062.1: 231,598-248,753 , GRCh37.p13 chr6: 112,555,278-112,572,434 LAMA4, LAMA4-AS1
    nsv6816135copy number variation1nstd229human GRCh38 chr6: 112,157,862-112,163,405 , GRCh37.p13 chr6|NW_003871062.1: 155,383-160,926 , GRCh37.p13 chr6: 112,479,064-112,484,607 LAMA4
    nsv6815593copy number variation1nstd229human GRCh38 chr6: 112,221,401-112,366,500 , GRCh37.p13 chr6: 112,586,594-112,687,702 RPSAP45, LAMA4-AS1, 6 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6811453copy number variation1nstd229human GRCh38 chr6: 112,172,741-112,177,685 , GRCh37.p13 chr6|NW_003871062.1: 170,262-175,206 , GRCh37.p13 chr6: 112,493,943-112,498,887 LAMA4
    nsv6811333copy number variation1nstd229human GRCh38 chr6: 112,160,874-112,161,041 , GRCh37.p13 chr6: 112,482,076-112,482,243 , GRCh37.p13 chr6|NW_003871062.1: 158,395-158,562 LAMA4
    nsv6811134copy number variation1nstd229human GRCh38 chr6: 112,109,644-112,109,807 , GRCh37.p13 chr6|NW_003871062.1: 107,166-107,329 , GRCh37.p13 chr6: 112,430,847-112,431,010 LAMA4
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