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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7147796insertion1nstd232human GRCh37.p13 chr2: 202,279,656-202,279,656 , GRCh38.p12 chr2: 201,414,933-201,414,933 TRAK2
    nsv7049459inversion1nstd229human GRCh38 chr2: 199,624,566-202,238,851 , GRCh37.p13 chr2: 200,489,289-203,103,574 LOC105373833, NDUFB3, 76 more genes
    nsv7048491inversion1nstd229human GRCh38 chr2: 201,421,764-201,421,824 , GRCh37.p13 chr2: 202,286,487-202,286,547 TRAK2
    nsv7038636inversion1nstd229human GRCh38 chr2: 201,436,987-201,440,317 , GRCh37.p13 chr2: 202,301,710-202,305,040 TRAK2
    nsv6697641copy number variation1nstd229human GRCh38 chr2: 201,386,456-201,393,208 , GRCh37.p13 chr2: 202,251,179-202,257,931 TRAK2
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6688178copy number variation1nstd229human GRCh38 chr2: 201,359,101-201,391,200 , GRCh37.p13 chr2: 202,223,824-202,255,923 FLACC1, TRAK2
    nsv6683523copy number variation1nstd229human GRCh38 chr2: 201,436,440-201,436,571 , GRCh37.p13 chr2: 202,301,163-202,301,294 TRAK2
    nsv6682208copy number variation1nstd229human GRCh38 chr2: 201,441,475-201,447,211 , GRCh37.p13 chr2: 202,306,198-202,311,934 TRAK2
    nsv6680043copy number variation1nstd229human GRCh38 chr2: 201,424,401-201,435,600 , GRCh37.p13 chr2: 202,289,124-202,300,323 TRAK2
    nsv6679260copy number variation1nstd229human GRCh38 chr2: 201,342,198-201,398,770 , GRCh37.p13 chr2: 202,206,921-202,263,493 FLACC1, TRAK2
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6537851inversion1nstd223human GRCh38 chr2: 201,449,654-201,450,221 , GRCh37.p13 chr2: 202,314,377-202,314,944 STRADB, TRAK2
    nsv6350181copy number variation1nstd223human GRCh38 chr2: 201,392,001-201,392,900 , GRCh37.p13 chr2: 202,256,724-202,257,623 TRAK2
    nsv6346208copy number variation1nstd223human GRCh38 chr2: 201,442,349-201,450,325 , GRCh37.p13 chr2: 202,307,072-202,315,048 STRADB, TRAK2
    nsv6342836copy number variation1nstd223human GRCh38 chr2: 201,441,469-201,447,210 , GRCh37.p13 chr2: 202,306,192-202,311,933 TRAK2
    nsv6336880copy number variation1nstd223human GRCh38 chr2: 201,380,208-201,382,839 , GRCh37.p13 chr2: 202,244,931-202,247,562 TRAK2
    nsv6336140copy number variation1nstd223human GRCh38 chr2: 201,379,906-201,380,396 , GRCh37.p13 chr2: 202,244,629-202,245,119 TRAK2
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
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