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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948988insertion1nstd209human GRCh38 chr7: 92,261,377-92,261,377 , GRCh37.p13 chr7: 91,890,691-91,890,691 ANKIB1
    nsv5915328copy number variation1nstd209human GRCh38 chr7: 92,374,975-92,375,078 , GRCh37.p13 chr7: 92,004,289-92,004,392 ANKIB1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487468copy number variation1nstd206human GRCh38 chr7: 92,374,976-92,375,079 , GRCh37.p13 chr7: 92,004,290-92,004,393 ANKIB1
    nsv5486738copy number variation1nstd206human GRCh38 chr7: 92,365,529-92,367,046 , GRCh37.p13 chr7: 91,994,843-91,996,360 ANKIB1
    nsv5484552copy number variation1nstd206human GRCh38 chr7: 92,351,095-92,352,473 , GRCh37.p13 chr7: 91,980,409-91,981,787 ANKIB1
    nsv5477490copy number variation1nstd206human GRCh38 chr7: 92,397,860-92,398,205 , GRCh37.p13 chr7: 92,027,174-92,027,519 ANKIB1
    nsv5476769copy number variation1nstd206human GRCh38 chr7: 92,390,116-92,391,165 , GRCh37.p13 chr7: 92,019,430-92,020,479 ANKIB1
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5370783translocation1nstd200human GRCh38 chr7: 92,295,167-92,295,167 , GRCh38 chr7: 92,307,357-92,307,357 , GRCh37.p13 chr7: 91,924,481-91,924,481 , GRCh37.p13 chr7: 91,936,671-91,936,671 ANKIB1
    nsv5370782translocation1nstd200human GRCh38 chr7: 92,246,519-92,246,519 , GRCh38 chr7: 92,294,888-92,294,888 , GRCh37.p13 chr7: 91,924,202-91,924,202 , GRCh37.p13 chr7: 91,875,833-91,875,833 ANKIB1, KRIT1
    nsv5347273translocation1nstd200human GRCh38 chr7: 92,246,024-92,246,024 , GRCh38 chr8: 61,787,913-61,787,913 , GRCh37.p13 chr7: 91,875,338-91,875,338 , GRCh37.p13 chr8: 62,700,472-62,700,472 KRIT1, ANKIB1, 1 more genes
    nsv5343899translocation1nstd200human GRCh37 chr7: 91,936,671-91,936,671 , GRCh37 chr7: 91,924,481-91,924,481 , GRCh38.p12 chr7: 92,295,167-92,295,167 , GRCh38.p12 chr7: 92,307,357-92,307,357 ANKIB1
    nsv5336417translocation1nstd200human GRCh37 chr7: 91,875,338-91,875,338 , GRCh37 chr8: 62,700,472-62,700,472 , GRCh38.p12 chr7: 92,246,024-92,246,024 , GRCh38.p12 chr8: 61,787,913-61,787,913 KRIT1, ANKIB1, 1 more genes
    nsv5330087translocation1nstd200human GRCh37 chr7: 91,875,833-91,875,833 , GRCh37 chr7: 91,924,202-91,924,202 , GRCh38.p12 chr7: 92,246,519-92,246,519 , GRCh38.p12 chr7: 92,294,888-92,294,888 ANKIB1, KRIT1
    nsv5329783translocation1nstd200human GRCh37 chr7: 92,019,430-92,019,430 , GRCh37 chr7: 92,020,479-92,020,479 , GRCh38.p12 chr7: 92,390,116-92,390,116 , GRCh38.p12 chr7: 92,391,165-92,391,165 ANKIB1
    nsv5324682translocation1nstd204human GRCh38.p13 chr7: 92,295,167-92,295,167 , GRCh38.p13 chr7: 92,307,357-92,307,357 , GRCh37.p13 chr7: 91,924,481-91,924,481 , GRCh37.p13 chr7: 91,936,671-91,936,671 ANKIB1
    nsv5320701translocation1nstd204human GRCh38.p13 chr8: 61,787,913-61,787,913 , GRCh37.p13 chr8: 62,700,472-62,700,472 , GRCh37.p13 chr7: 91,875,338-91,875,338 , GRCh38.p13 chr7: 92,246,024-92,246,024 KRIT1, ANKIB1, 1 more genes
    nsv5308011copy number variation1nstd204human GRCh38.p13 chr7: 92,254,762-92,255,562 , GRCh37.p13 chr7: 91,884,076-91,884,876 ANKIB1
    nsv5249853copy number variation1nstd204human GRCh38.p13 chr7: 92,333,301-92,337,600 , GRCh37.p13 chr7: 91,962,615-91,966,914 ANKIB1
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