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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095446copy number variation1nstd102humanLikely benign GRCh37 chr18: 48,573,397-48,573,685 , GRCh38.p12 chr18: 51,047,027-51,047,315 SMAD4
    nsv7095384copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,602,988-48,604,837 , GRCh38.p12 chr18: 51,076,618-51,078,467 SMAD4
    nsv7095250copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,591,783-48,593,567 , GRCh38.p12 chr18: 51,065,413-51,067,197 SMAD4
    nsv7093172copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 48,556,994-48,573,471 , GRCh38.p12 chr18: 51,030,624-51,047,101 SMAD4
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7015093copy number variation1nstd229human GRCh38 chr18: 51,078,201-51,079,800 , GRCh37.p13 chr18: 48,604,571-48,606,170 SMAD4
    nsv7009845copy number variation1nstd229human GRCh38 chr18: 51,038,117-51,040,978 , GRCh37.p13 chr18: 48,564,487-48,567,348 SMAD4
    nsv7009748copy number variation1nstd229human GRCh38 chr18: 51,012,401-51,031,400 , GRCh37.p13 chr18: 48,538,771-48,557,770 SMAD4
    nsv7003570copy number variation1nstd229human GRCh38 chr18: 50,884,950-51,036,179 , GRCh37.p13 chr18: 48,411,320-48,562,549 LOC107985152, ME2, 2 more genes
    nsv6637893copy number variation1nstd102humanUncertain significance GRCh37 chr18: 48,273,185-51,134,173 , GRCh38.p12 chr18: 50,746,815-53,607,803 LOC105372121, LOC100420949, 23 more genes
    nsv6624595copy number variation1nstd224human GRCh37 chr18: 48,573,424-48,611,975 , GRCh38.p12 chr18: 51,047,054-51,085,605 SMAD4
    nsv6595020inversion1nstd223human GRCh38 chr18: 49,148,101-52,144,680 , GRCh37.p13 chr18: 46,674,471-49,671,050 MYO5B, LIPG, 49 more genes
    nsv6528994copy number variation1nstd223human GRCh38 chr18: 51,029,201-51,032,400 , GRCh37.p13 chr18: 48,555,571-48,558,770 SMAD4
    nsv6528590copy number variation1nstd223human GRCh38 chr18: 51,029,701-51,031,300 , GRCh37.p13 chr18: 48,556,071-48,557,670 SMAD4
    nsv6524390copy number variation1nstd223human GRCh38 chr18: 51,045,201-51,047,400 , GRCh37.p13 chr18: 48,571,571-48,573,770 SMAD4
    nsv6522206copy number variation1nstd223human GRCh38 chr18: 51,071,057-51,071,665 , GRCh37.p13 chr18: 48,597,427-48,598,035 SMAD4
    nsv6521973copy number variation1nstd223human GRCh38 chr18: 51,076,776-51,078,255 , GRCh37.p13 chr18: 48,603,146-48,604,625 SMAD4
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
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