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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056809inversion1nstd229human GRCh38 chr3: 18,903,604-20,316,545 , GRCh37.p13 chr3: 18,945,096-20,358,037 SGO1-AS1, HSPA8P18, 19 more genes
    nsv7054116inversion1nstd229human GRCh38 chr3: 19,170,573-20,582,118 , GRCh37.p13 chr3: 19,212,065-20,623,610 SGO1, EFHB, 17 more genes
    nsv7051519inversion1nstd229human GRCh38 chr3: 19,693,381-21,117,946 , GRCh37.p13 chr3: 19,734,873-21,159,438 LOC107986068, PP2D1, 16 more genes
    nsv7047955inversion1nstd229human GRCh38 chr3: 16,742,381-21,099,619 , GRCh37.p13 chr3: 16,783,888-21,141,111 PP2D1, TRC-GCA25-1, 37 more genes
    nsv7046868inversion1nstd229human GRCh38 chr3: 17,344,159-22,155,377 , GRCh37.p13 chr3: 17,385,651-22,196,869 LOC105376981, LOC107986066, 39 more genes
    nsv6717551copy number variation1nstd229human GRCh38 chr3: 19,967,264-20,074,983 , GRCh37.p13 chr3: 20,008,756-20,116,475 KAT2B, SAP18P3, 4 more genes
    nsv6713309copy number variation1nstd229human GRCh38 chr3: 19,970,001-19,973,200 , GRCh37.p13 chr3: 20,011,493-20,014,692 RAB5A
    nsv6706483copy number variation1nstd229human GRCh38 chr3: 19,937,472-20,021,665 , GRCh37.p13 chr3: 19,978,964-20,063,157 PP2D1, HSPA8P18, 5 more genes
    nsv6705854copy number variation1nstd229human GRCh38 chr3: 19,953,501-19,960,600 , GRCh37.p13 chr3: 19,994,993-20,002,092 RAB5A
    nsv6705042copy number variation1nstd229human GRCh38 chr3: 19,601,002-20,163,951 , GRCh37.p13 chr3: 19,642,494-20,205,443 KAT2B, SAP18P3, 9 more genes
    nsv6703622copy number variation1nstd229human GRCh38 chr3: 19,444,707-20,918,143 , GRCh37.p13 chr3: 19,486,199-20,959,635 RNU6-815P, SAP18P3, 17 more genes
    nsv6703209copy number variation1nstd229human GRCh38 chr3: 19,975,208-19,975,296 , GRCh37.p13 chr3: 20,016,700-20,016,788 RAB5A
    nsv6702780copy number variation1nstd229human GRCh38 chr3: 19,962,635-19,964,747 , GRCh37.p13 chr3: 20,004,127-20,006,239 RAB5A
    nsv6701667copy number variation1nstd229human GRCh38 chr3: 19,974,181-19,974,406 , GRCh37.p13 chr3: 20,015,673-20,015,898 RAB5A
    nsv6700930copy number variation1nstd229human GRCh38 chr3: 19,414,887-20,068,292 , GRCh37.p13 chr3: 19,456,379-20,109,784 RAB5A, LOC105376984, 9 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6628546copy number variation1nstd224human GRCh37 chr3: 18,235,724-20,185,009 , GRCh38.p12 chr3: 18,194,232-20,143,517 RAB5A, KAT2B, 19 more genes
    nsv6552470inversion1nstd223human GRCh38 chr3: 19,974,204-19,975,163 , GRCh37.p13 chr3: 20,015,696-20,016,655 RAB5A
    nsv6547881inversion1nstd223human GRCh38 chr3: 19,976,405-19,977,312 , GRCh37.p13 chr3: 20,017,897-20,018,804 RAB5A
    nsv6545573inversion1nstd223human GRCh38 chr3: 16,746,915-21,192,302 , GRCh37.p13 chr3: 16,788,422-21,233,794 TBC1D5, SATB1, 38 more genes
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