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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977915inversion1nstd209human GRCh38 chr7: 86,525,777-88,855,329 , GRCh37.p13 chr7: 86,155,093-88,484,643 , GRM3, 31 more genes
    nsv5917656copy number variation1nstd209human GRCh38 chr7: 87,374,848-87,374,930 , GRCh37.p13 chr7: 87,004,164-87,004,246 CROT
    nsv5915095copy number variation1nstd209human GRCh38 chr7: 87,345,722-87,346,386 , GRCh37.p13 chr7: 86,975,038-86,975,702 TP53TG1, CROT
    nsv5913107copy number variation1nstd209human GRCh38 chr7: 87,398,302-87,512,194 , GRCh37.p13 chr7: 87,027,618-87,141,510 ABCB1, ABCB4, 1 more genes
    nsv5850017copy number variation1nstd209human GRCh38 chr7: 87,397,738-87,425,639 , GRCh37.p13 chr7: 87,027,054-87,054,955 CROT, ABCB4
    nsv5683322mobile element insertion2nstd211human GRCh38 chr7: 87,351,527-87,351,527 , GRCh37.p13 chr7: 86,980,843-86,980,843 CROT
    nsv5630238insertion1nstd207human GRCh38 chr7: 87,380,245-87,380,245 , GRCh37.p13 chr7: 87,009,561-87,009,561 CROT
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5552885insertion1nstd206human GRCh38 chr7: 87,352,227-87,352,261 , GRCh37.p13 chr7: 86,981,543-86,981,577 CROT
    nsv5482934copy number variation1nstd206human GRCh38 chr7: 87,380,245-87,380,395 , GRCh37.p13 chr7: 87,009,561-87,009,711 CROT
    nsv5481880copy number variation1nstd206human GRCh38 chr7: 87,374,848-87,374,931 , GRCh37.p13 chr7: 87,004,164-87,004,247 CROT
    nsv5405418mobile element insertion1nstd206human GRCh38 chr7: 87,351,527-87,351,578 , GRCh37.p13 chr7: 86,980,843-86,980,894 CROT
    nsv5386909copy number variation2nstd186human GRCh37 chr7: 87,009,561-87,009,711 , GRCh38.p12 chr7: 87,380,245-87,380,395 CROT
    nsv5386636copy number variation1nstd186human GRCh37 chr7: 87,009,561-87,009,710 , GRCh38.p12 chr7: 87,380,245-87,380,394 CROT
    nsv5363938translocation1nstd200human GRCh38 chr7: 87,374,848-87,374,848 , GRCh38 chr7: 87,374,931-87,374,931 , GRCh37.p13 chr7: 87,004,164-87,004,164 , GRCh37.p13 chr7: 87,004,247-87,004,247 CROT
    nsv5313127copy number variation1nstd204human GRCh38.p13 chr7: 87,380,244-87,380,395 , GRCh37.p13 chr7: 87,009,560-87,009,711 CROT
    nsv5171385mobile element insertion1nstd203human GRCh38 chr7: 87,346,621-87,346,635 , GRCh37.p13 chr7: 86,975,937-86,975,951 CROT
    nsv5107366mobile element insertion1nstd203human GRCh38 chr7: 87,351,513-87,351,524 , GRCh37.p13 chr7: 86,980,829-86,980,840 CROT
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
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