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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
    nsv7096951copy number variation2nstd102humanUncertain significance GRCh37 chr3: 186,256,485-187,009,420 , GRCh38.p12 chr3: 186,538,696-187,291,632 AHSG, ST6GAL1, 32 more genes
    nsv7047831inversion1nstd229human GRCh38 chr3: 186,728,446-186,729,589 , GRCh37.p13 chr3: 186,446,235-186,447,378 KNG1
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6735365copy number variation1nstd229human GRCh38 chr3: 186,719,562-186,721,186 , GRCh37.p13 chr3: 186,437,351-186,438,975 KNG1
    nsv6731232copy number variation1nstd229human GRCh38 chr3: 186,406,559-187,159,867 , GRCh37.p13 chr3: 186,124,348-186,877,655 PET100P1, SNORA81, 30 more genes
    nsv6730395copy number variation1nstd229human GRCh38 chr3: 186,724,183-186,724,237 , GRCh37.p13 chr3: 186,441,972-186,442,026 KNG1
    nsv6726794copy number variation1nstd229human GRCh38 chr3: 186,670,823-186,733,876 , GRCh37.p13 chr3: 186,388,612-186,451,665 HRGP1, HRG-AS1, 2 more genes
    nsv6721763copy number variation1nstd229human GRCh38 chr3: 186,726,283-186,726,302 , GRCh37.p13 chr3: 186,444,072-186,444,091 KNG1
    nsv6720977copy number variation1nstd229human GRCh38 chr3: 186,735,602-186,774,241 , GRCh37.p13 chr3: 186,453,391-186,492,030 GPS2P2, RNU6-1105P, 2 more genes
    nsv6718933copy number variation1nstd229human GRCh38 chr3: 186,740,968-186,741,372 , GRCh37.p13 chr3: 186,458,757-186,459,161 KNG1
    nsv6636645copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 184,170,962-188,047,867 , GRCh38.p12 chr3: 184,453,174-188,330,079 AHSG, BCL6, 80 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628929copy number variation1nstd224human GRCh37 chr3: 186,328,121-186,710,637 , GRCh38.p12 chr3: 186,610,332-186,992,849 AHSG, EIF4A2, 21 more genes
    nsv6565470inversion1nstd223human GRCh38 chr3: 186,729,771-186,730,448 , GRCh37.p13 chr3: 186,447,560-186,448,237 KNG1
    nsv6369465copy number variation1nstd223human GRCh38 chr3: 186,736,909-186,737,997 , GRCh37.p13 chr3: 186,454,698-186,455,786 KNG1
    nsv6361622copy number variation1nstd223human GRCh38 chr3: 186,719,497-186,721,184 , GRCh37.p13 chr3: 186,437,286-186,438,973 KNG1
    nsv6361243copy number variation1nstd223human GRCh38 chr3: 186,688,722-186,778,386 , GRCh37.p13 chr3: 186,406,511-186,496,175 KNG1, HRGP1, 4 more genes
    nsv6359274copy number variation1nstd223human GRCh38 chr3: 186,723,950-186,724,860 , GRCh37.p13 chr3: 186,441,739-186,442,649 KNG1
    nsv6356801copy number variation1nstd223human GRCh38 chr3: 186,735,411-186,736,767 , GRCh37.p13 chr3: 186,453,200-186,454,556 KNG1
    nsv6356763copy number variation1nstd223human GRCh38 chr3: 186,742,749-186,764,716 , GRCh37.p13 chr3: 186,460,538-186,482,505 KNG1, PSMD10P2
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