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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976512inversion1nstd209human GRCh38 chr7: 5,976,108-6,745,714 , GRCh37.p13 chr7: 6,015,739-6,785,345 PMS2, RAC1, 22 more genes
    nsv5911322copy number variation1nstd209human GRCh38 chr7: 6,421,670-7,105,388 , GRCh37.p13 chr7: 6,461,301-7,145,019 , GRID2IP, 25 more genes
    nsv5667605inversion1nstd207human GRCh37.p13 chr7: 6,028,678-6,775,274 , GRCh38 chr7: 5,989,047-6,735,643 PMS2, RAC1, 22 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554365sequence alteration1nstd206human GRCh38 chr7: 5,895,867-6,829,202 , GRCh37.p13 chr7: 5,935,498-6,868,833 , RAC1, 28 more genes
    nsv5472427copy number variation1nstd206human GRCh38 chr7: 6,646,599-6,648,919 , GRCh37.p13 chr7: 6,686,230-6,688,550 ZNF316
    nsv5370167translocation1nstd200human GRCh38 chr7: 6,648,919-6,648,919 , GRCh38 chr7: 6,646,599-6,646,599 , GRCh37.p13 chr7: 6,686,230-6,686,230 , GRCh37.p13 chr7: 6,688,550-6,688,550 ZNF316
    nsv5229919copy number variation1nstd204human GRCh38.p13 chr7: 6,314,201-6,774,600 , GRCh37.p13 chr7: 6,353,832-6,814,231 GRID2IP, PMS2CL, 14 more genes
    nsv4953314copy number variation1nstd200human GRCh38 chr7: 6,577,774-6,731,178 , GRCh37.p13 chr7: 6,617,405-6,770,809 ZDHHC4, ZNF853, 4 more genes
    nsv4953307copy number variation1nstd200human GRCh38 chr7: 6,207,809-6,651,290 , GRCh37.p13 chr7: 6,247,440-6,690,921 ZNF853, DAGLB, 11 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4828721copy number variation1nstd200human GRCh37 chr7: 6,617,405-6,770,809 , GRCh38.p12 chr7: 6,577,774-6,731,178 ZDHHC4, ZNF316, 4 more genes
    nsv4818641copy number variation1nstd200human GRCh37 chr7: 6,686,230-6,688,550 , GRCh38.p12 chr7: 6,646,599-6,648,919 ZNF316
    nsv4730107inversion8nstd198human GRCh37.p13 chr7: 5,881,319-6,860,546 , GRCh38 chr7: 5,841,688-6,820,915 , PMS2, 31 more genes
    nsv4729679copy number variation1nstd102humanUncertain significance GRCh37 chr7: 5,919,587-6,762,394 , GRCh38.p12 chr7: 5,879,956-6,722,763 ZDHHC4, LOC100419773, 24 more genes
    nsv4729020copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,183,858-7,137,555 , GRCh38.p12 chr7: 6,144,227-7,097,924 GRID2IP, FAM86LP, 29 more genes
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4675329copy number variation1nstd102humanUncertain significance GRCh37 chr7: 6,394,921-6,762,394 , GRCh38.p12 chr7: 6,355,290-6,722,763 RAC1, LOC100419773, 11 more genes
    nsv4674972copy number variation1nstd102humanLikely benign GRCh37 chr7: 6,536,635-7,639,607 , GRCh38.p12 chr7: 6,497,004-7,599,976 ZNF853, LOC105375138, 27 more genes
    nsv4657995inversion1nstd185human GRCh37.p13 chr7: 6,032,437-6,774,174 , GRCh38.p13 chr7: 5,992,806-6,734,543 PMS2, RAC1, 22 more genes
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