U.S. flag

An official website of the United States government

Links from Gene

Items: 1 to 20 of 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7045773inversion1nstd229human GRCh38 chr7: 100,499,070-100,696,514 , GRCh37.p13 chr7: 100,096,693-100,294,137 AGFG2, LOC105375429, 13 more genes
    nsv6837767copy number variation1nstd229human GRCh38 chr7: 100,603,658-100,679,521 , GRCh37.p13 chr7: 100,201,281-100,277,144 PCOLCE-AS1, LOC105375429, 6 more genes
    nsv6829600copy number variation1nstd229human GRCh38 chr7: 100,591,618-100,623,863 , GRCh37.p13 chr7: 100,189,241-100,221,486 PCOLCE, TFR2, 3 more genes
    nsv6822884copy number variation1nstd229human GRCh38 chr7: 100,573,701-100,682,700 , GRCh37.p13 chr7: 100,171,324-100,280,323 PCOLCE-AS1, GIGYF1, 9 more genes
    nsv6820511copy number variation1nstd229human GRCh38 chr7: 100,411,473-102,072,572 , GRCh37.p13 chr7: 100,009,096-101,715,852 MIR4653, UFSP1, 63 more genes
    nsv6818312copy number variation1nstd229human GRCh38 chr7: 100,547,001-100,919,000 , GRCh37.p13 chr7: 100,144,624-100,516,620 TRIP6, MIR6875, 24 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6616460copy number variation1nstd223human GRCh38 chr7: 100,589,426-100,590,876 , GRCh37.p13 chr7: 100,187,049-100,188,499 PCOLCE-AS1, FBXO24
    nsv6614776copy number variation1nstd223human GRCh38 chr7: 99,943,801-101,566,300 , GRCh37.p13 chr7: 99,541,424-101,209,580 MUC12, FBXO24, 95 more genes
    nsv6610980copy number variation1nstd223human GRCh38 chr7: 100,548,101-100,840,100 , GRCh37.p13 chr7: 100,145,724-100,437,722 LRCH4, MOSPD3, 18 more genes
    nsv6607668copy number variation1nstd223human GRCh38 chr7: 100,428,001-100,907,900 , GRCh37.p13 chr7: 100,025,624-100,505,520 LOC107986829, FBXO24, 33 more genes
    nsv6607287copy number variation1nstd223human GRCh38 chr7: 100,592,639-100,609,816 , GRCh37.p13 chr7: 100,190,262-100,207,439 PCOLCE, FBXO24, 1 more genes
    nsv6604708copy number variation1nstd223human GRCh38 chr7: 100,460,230-101,238,868 , GRCh37.p13 chr7: 100,057,853-100,882,149 RN7SKP54, ZNHIT1, 49 more genes
    nsv6601439copy number variation1nstd223human GRCh38 chr7: 100,412,401-100,918,900 , GRCh37.p13 chr7: 100,010,024-100,516,520 TSC22D4, NYAP1, 33 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center
    External link. Please review our privacy policy.