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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147705copy number variation1nstd232human GRCh37.p13 chr1: 201,893,585-201,893,652 , GRCh38.p12 chr1: 201,924,457-201,924,524 LMOD1
    nsv7099256copy number variation1nstd231human GRCh38.p12 chr1: 201,916,209-203,311,623 , GRCh37 chr1: 201,885,337-203,280,751 ADORA1, CHI3L1, 49 more genes
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7048044inversion1nstd229human GRCh38 chr1: 200,722,696-202,712,068 , GRCh37.p13 chr1: 200,691,824-202,681,196 ARL8A, KIF21B, 52 more genes
    nsv6676156copy number variation1nstd229human GRCh38 chr1: 201,916,726-201,925,504 , GRCh37.p13 chr1: 201,885,854-201,894,632 LMOD1
    nsv6674715copy number variation1nstd229human GRCh38 chr1: 201,901,187-201,952,212 , GRCh37.p13 chr1: 201,870,315-201,921,340 LMOD1
    nsv6670641copy number variation1nstd229human GRCh38 chr1: 201,907,252-201,914,083 , GRCh37.p13 chr1: 201,876,380-201,883,211 LMOD1
    nsv6669782copy number variation1nstd229human GRCh38 chr1: 201,900,751-201,946,078 , GRCh37.p13 chr1: 201,869,879-201,915,206 LMOD1
    nsv6667747copy number variation1nstd229human GRCh38 chr1: 201,936,888-202,137,804 , GRCh37.p13 chr1: 201,906,016-202,106,932 RPL10P4, ELF3-AS1, 11 more genes
    nsv6664131copy number variation1nstd229human GRCh38 chr1: 201,918,212-201,918,273 , GRCh37.p13 chr1: 201,887,340-201,887,401 LMOD1
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6547281inversion1nstd223human GRCh38 chr1: 201,935,160-201,936,223 , GRCh37.p13 chr1: 201,904,288-201,905,351 LMOD1
    nsv6322630copy number variation1nstd223human GRCh38 chr1: 201,928,800-201,935,753 , GRCh37.p13 chr1: 201,897,928-201,904,881 LMOD1
    nsv6320636copy number variation1nstd223human GRCh38 chr1: 201,907,252-201,914,079 , GRCh37.p13 chr1: 201,876,380-201,883,207 LMOD1
    nsv6314229complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr1: 201,894,853-201,894,853 , GRCh38.p12 chr1: 201,894,853-201,894,853 , GRCh38.p12 chr1: 239,985,723-239,985,723 , GRCh38.p12 chr1: 239,985,728-239,985,728 , GRCh37 chr1: 201,863,981-201,863,981 , GRCh37 chr1: 201,863,981-201,863,981 , GRCh37 chr1: 240,149,023-240,149,023 , GRCh37 chr1: 240,149,028-240,149,028 LMOD1
    nsv6163722copy number variation1nstd214human GRCh38 chr1: 201,924,395-201,924,498 , GRCh37.p13 chr1: 201,893,523-201,893,626 LMOD1
    nsv6161928copy number variation1nstd214human GRCh38 chr1: 201,901,624-201,901,685 , GRCh37.p13 chr1: 201,870,752-201,870,813 LMOD1
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