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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv6769330copy number variation1nstd229human GRCh38 chr5: 73,445,201-73,446,600 , GRCh37.p13 chr5: 72,741,028-72,742,427 FOXD1
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6415089copy number variation1nstd223human GRCh38 chr5: 73,443,901-73,448,500 , GRCh37.p13 chr5: 72,739,728-72,744,325 FOXD1
    nsv6412700copy number variation1nstd223human GRCh38 chr5: 73,401,701-73,469,800 , GRCh37.p13 chr5: 72,697,528-72,765,625 FOXD1, LINC01386, 1 more genes
    nsv6412439copy number variation1nstd223human GRCh38 chr5: 73,415,101-73,454,500 , GRCh37.p13 chr5: 72,710,928-72,750,325 FOXD1, LINC01386
    nsv6412118copy number variation1nstd223human GRCh38 chr5: 73,445,301-73,448,700 , GRCh37.p13 chr5: 72,741,128-72,744,525 FOXD1
    nsv6407886copy number variation1nstd223human GRCh38 chr5: 73,448,601-73,454,800 , GRCh37.p13 chr5: 72,744,426-72,750,625 FOXD1, LINC01386
    nsv6404132copy number variation1nstd223human GRCh38 chr5: 73,435,801-73,543,400 , GRCh37.p13 chr5: 72,731,628-72,839,225 LINC01386, BTF3, 2 more genes
    nsv6396459copy number variation1nstd223human GRCh38 chr5: 73,446,601-73,451,400 , GRCh37.p13 chr5: 72,742,428-72,747,225 FOXD1
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv5902422copy number variation1nstd209human GRCh38 chr5: 73,384,899-73,445,669 , GRCh37.p13 chr5: 72,680,726-72,741,496 FOXD1, LOC107986383
    nsv4591585copy number variation1nstd183human GRCh37 chr5: 72,742,655-72,744,608 , GRCh38.p12 chr5: 73,446,828-73,448,783 FOXD1
    nsv4591584copy number variation1nstd183human GRCh37 chr5: 72,742,598-72,744,615 , GRCh38.p12 chr5: 73,446,771-73,448,790 FOXD1
    nsv4591583copy number variation1nstd183human GRCh37 chr5: 72,733,703-72,836,482 , GRCh38.p12 chr5: 73,437,876-73,540,657 FOXD1, LINC01386, 2 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
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