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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv6992802copy number variation1nstd229human GRCh38 chr16: 57,415,901-57,529,100 , GRCh37.p13 chr16: 57,449,813-57,563,012 DOK4, COQ9, 5 more genes
    nsv6990163copy number variation1nstd229human GRCh38 chr16: 57,571,435-57,574,754 , GRCh37.p13 chr16: 57,605,347-57,608,666 LOC105371291, ADGRG5
    nsv6989380copy number variation1nstd229human GRCh38 chr16: 57,569,258-57,569,923 , GRCh37.p13 chr16: 57,603,170-57,603,835 LOC105371291, ADGRG5
    nsv6988347copy number variation1nstd229human GRCh38 chr16: 57,545,118-57,560,049 , GRCh37.p13 chr16: 57,579,030-57,593,961 ADGRG5
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 more genes
    nsv6986871copy number variation1nstd229human GRCh38 chr16: 57,525,101-57,537,400 , GRCh37.p13 chr16: 57,559,013-57,571,312 ADGRG5, CCDC102A
    nsv6984982copy number variation1nstd229human GRCh38 chr16: 57,555,877-57,744,440 , GRCh37.p13 chr16: 57,589,789-57,774,021 HMGB3P32, LOC107984889, 8 more genes
    nsv6978535copy number variation1nstd229human GRCh38 chr16: 57,188,715-57,538,791 , GRCh37.p13 chr16: 57,222,627-57,572,703 CX3CL1, ARL2BP, 13 more genes
    nsv6978346copy number variation1nstd229human GRCh38 chr16: 57,543,574-57,573,974 , GRCh37.p13 chr16: 57,577,486-57,607,886 LOC105371291, ADGRG5
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623868copy number variation1nstd224human GRCh37 chr16: 57,589,057-57,607,007 , GRCh38.p12 chr16: 57,555,145-57,573,095 ADGRG5, LOC105371291
    nsv6623681copy number variation2nstd224human GRCh37 chr16: 57,591,985-57,604,429 , GRCh38.p12 chr16: 57,558,073-57,570,517 ADGRG5, LOC105371291
    nsv6509903copy number variation1nstd223human GRCh38 chr16: 57,527,201-57,529,400 , GRCh37.p13 chr16: 57,561,113-57,563,312 ADGRG5, CCDC102A
    nsv6508147copy number variation1nstd223human GRCh38 chr16: 57,545,118-57,560,048 , GRCh37.p13 chr16: 57,579,030-57,593,960 ADGRG5
    nsv6507537copy number variation1nstd223human GRCh38 chr16: 57,571,435-57,574,754 , GRCh37.p13 chr16: 57,605,347-57,608,666 LOC105371291, ADGRG5
    nsv6507154copy number variation1nstd223human GRCh38 chr16: 57,568,521-57,569,176 , GRCh37.p13 chr16: 57,602,433-57,603,088 LOC105371291, ADGRG5
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
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