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Items: 1 to 20 of 1450

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146426copy number variation1nstd232human GRCh37.p13 chr12: 132,697,666-132,697,823 , GRCh38.p12 chr12: 132,213,121-132,213,278 GALNT9
    nsv7146225copy number variation1nstd232human GRCh37.p13 chr12: 132,697,746-132,697,823 , GRCh38.p12 chr12: 132,213,201-132,213,278 GALNT9
    nsv7145633insertion1nstd232human GRCh37.p13 chr12: 132,897,214-132,897,214 , GRCh38.p12 chr12: 132,320,628-132,320,628 GALNT9
    nsv7145220copy number variation1nstd232human GRCh37.p13 chr12: 132,868,239-132,868,313 , GRCh38.p12 chr12: 132,291,653-132,291,727 GALNT9
    nsv7144392insertion1nstd232human GRCh37.p13 chr12: 132,871,216-132,871,216 , GRCh38.p12 chr12: 132,294,630-132,294,630 GALNT9
    nsv7142167insertion1nstd232human GRCh37.p13 chr12: 132,819,452-132,819,452 , GRCh38.p12 chr12: 132,243,392-132,243,392 GALNT9
    nsv7139853copy number variation1nstd232human GRCh37.p13 chr12: 132,879,981-132,880,108 , GRCh38.p12 chr12: 132,303,395-132,303,522 GALNT9
    nsv7137716insertion1nstd232human GRCh37.p13 chr12: 132,821,359-132,821,359 , GRCh38.p12 chr12: 132,244,806-132,244,806 GALNT9
    nsv7099028copy number variation1nstd102humanUncertain significance GRCh38 chr12: 132,237,283-132,491,257 , GRCh37.p13 chr12|NW_003315937.1: 11,322-165,247 , GRCh37.p13 chr12: 132,808,130-132,967,794 LOC105370092, LOC112268102, 5 more genes
    nsv7093960copy number variation1nstd102humanUncertain significance GRCh37 chr12: 132,414,268-133,263,901 , GRCh38.p12 chr12: 131,929,723-132,687,315 LOC107987169, NOC4L, 20 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7073229inversion1nstd229human GRCh38 chr12: 132,098,464-132,282,395 , GRCh37.p13 chr12: 132,583,009-132,706,992 DDX51, LINC02361, 6 more genes
    nsv7072321inversion1nstd229human GRCh38 chr12: 131,976,015-132,309,484 , GRCh37.p13 chr12: 132,460,560-132,706,992 LOC105370091, NOC4L, 8 more genes
    nsv7071385inversion1nstd229human GRCh38 chr12: 131,514,757-132,281,110 , GRCh37.p13 chr12: 131,999,302-132,706,992 LINC02361, EP400, 24 more genes
    nsv7069228inversion1nstd229human GRCh38 chr12: 131,736,676-132,414,978 , GRCh37.p13 chr12: 132,221,221-132,991,564 LOC107987169, NOC4L, 17 more genes
    nsv7067298inversion1nstd229human GRCh38 chr12: 132,079,777-132,851,356 , GRCh37.p13 chr12: 132,564,322-133,427,942 LRCOL1, PGAM5, 26 more genes
    nsv7062264inversion1nstd229human GRCh38 chr12: 132,291,934-132,360,612 , GRCh37.p13 chr12: 132,868,520-132,937,198 , GRCh37.p13 chr12|NW_003315937.1: 65,973-134,651 LOC101928416, GALNT9
    nsv7058684inversion1nstd229human GRCh38 chr12: 132,261,544-132,273,569 , GRCh37.p13 chr12|NW_003315937.1: 35,583-47,608 , GRCh37.p13 chr12: 132,838,130-132,850,155 GALNT9-AS1, GALNT9
    nsv6937196copy number variation1nstd229human GRCh38 chr12: 132,308,846-132,308,917 , GRCh37.p13 chr12|NW_003315937.1: 82,885-82,956 , GRCh37.p13 chr12: 132,885,432-132,885,503 GALNT9
    nsv6935815copy number variation1nstd229human GRCh38 chr12: 132,267,216-132,267,247 , GRCh37.p13 chr12: 132,843,802-132,843,833 , GRCh37.p13 chr12|NW_003315937.1: 41,255-41,286 GALNT9
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