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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144145insertion1nstd232human GRCh37.p13 chr1: 201,158,392-201,158,392 , GRCh38.p12 chr1: 201,189,264-201,189,264 IGFN1
    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
    nsv6677878copy number variation1nstd229human GRCh38 chr1: 200,974,330-201,208,004 , GRCh37.p13 chr1: 200,943,458-201,177,132 KIF21B, CACNA1S, 4 more genes
    nsv6675860copy number variation1nstd229human GRCh38 chr1: 201,186,706-201,214,568 , GRCh37.p13 chr1: 201,155,834-201,183,696 IGFN1
    nsv6674605copy number variation1nstd229human GRCh38 chr1: 201,226,614-201,259,939 , GRCh37.p13 chr1: 201,195,742-201,229,067 IGFN1
    nsv6673647copy number variation1nstd229human GRCh38 chr1: 200,873,101-201,555,700 , GRCh37.p13 chr1: 200,842,229-201,524,828 GPR25, PHLDA3, 18 more genes
    nsv6672801copy number variation1nstd229human GRCh38 chr1: 201,185,761-201,189,442 , GRCh37.p13 chr1: 201,154,889-201,158,570 IGFN1
    nsv6672468copy number variation1nstd229human GRCh38 chr1: 201,205,170-201,206,893 , GRCh37.p13 chr1: 201,174,298-201,176,021 IGFN1
    nsv6665201copy number variation1nstd229human GRCh38 chr1: 201,189,207-201,189,273 , GRCh37.p13 chr1: 201,158,335-201,158,401 IGFN1
    nsv6662962copy number variation1nstd229human GRCh38 chr1: 201,158,462-201,226,157 , GRCh37.p13 chr1: 201,127,590-201,195,285 IGFN1, TMEM9
    nsv6662813copy number variation1nstd229human GRCh38 chr1: 201,228,750-201,272,744 , GRCh37.p13 chr1: 201,197,878-201,241,872 IGFN1
    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
    nsv6335313copy number variation1nstd223human GRCh38 chr1: 200,974,330-201,208,004 , GRCh37.p13 chr1: 200,943,458-201,177,132 ASCL5, IGFN1, 4 more genes
    nsv6333325copy number variation1nstd223human GRCh38 chr1: 201,195,296-201,196,438 , GRCh37.p13 chr1: 201,164,424-201,165,566 IGFN1
    nsv6327851copy number variation1nstd223human GRCh38 chr1: 201,209,580-201,210,984 , GRCh37.p13 chr1: 201,178,708-201,180,112 IGFN1
    nsv6325794copy number variation1nstd223human GRCh38 chr1: 201,185,761-201,189,435 , GRCh37.p13 chr1: 201,154,889-201,158,563 IGFN1
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