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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146798insertion1nstd232human GRCh37.p13 chr7: 87,009,711-87,009,711 , GRCh38.p12 chr7: 87,380,395-87,380,395 CROT
    nsv7054023inversion1nstd229human GRCh38 chr7: 87,371,586-87,371,652 , GRCh37.p13 chr7: 87,000,902-87,000,968 CROT
    nsv6837840copy number variation1nstd229human GRCh38 chr7: 87,356,699-87,357,200 , GRCh37.p13 chr7: 86,986,015-86,986,516 CROT
    nsv6831632copy number variation1nstd229human GRCh38 chr7: 86,090,518-87,706,185 , GRCh37.p13 chr7: 85,719,834-87,335,501 ABCB1, TP53TG1, 12 more genes
    nsv6828258copy number variation1nstd229human GRCh38 chr7: 87,380,245-87,380,395 , GRCh37.p13 chr7: 87,009,561-87,009,711 CROT
    nsv6823043copy number variation1nstd229human GRCh38 chr7: 87,373,573-87,375,721 , GRCh37.p13 chr7: 87,002,889-87,005,037 CROT
    nsv6822073copy number variation1nstd229human GRCh38 chr7: 86,140,900-87,353,128 , GRCh37.p13 chr7: 85,770,216-86,982,444 TMEM243, DMTF1, 8 more genes
    nsv6818739copy number variation1nstd229human GRCh38 chr7: 84,598,855-91,861,148 , GRCh37.p13 chr7: 84,228,171-91,490,462 CDK14, LOC101409256, 59 more genes
    nsv6818701copy number variation1nstd229human GRCh38 chr7: 87,353,419-87,357,152 , GRCh37.p13 chr7: 86,982,735-86,986,468 CROT
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632462copy number variation1nstd224human GRCh37 chr7: 86,944,642-87,517,349 , GRCh38.p12 chr7: 87,315,326-87,888,034 ABCB1, ABCB4, 6 more genes
    nsv6609121copy number variation1nstd223human GRCh38 chr7: 87,376,801-87,377,700 , GRCh37.p13 chr7: 87,006,117-87,007,016 CROT
    nsv6605769copy number variation1nstd223human GRCh38 chr7: 87,364,384-87,365,248 , GRCh37.p13 chr7: 86,993,700-86,994,564 CROT
    nsv6570364inversion1nstd223human GRCh38 chr7: 87,365,303-87,365,723 , GRCh37.p13 chr7: 86,994,619-86,995,039 CROT
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6303094copy number variation1nstd186human GRCh37 chr7: 87,004,164-87,004,247 , GRCh38.p12 chr7: 87,374,848-87,374,931 CROT
    nsv6177238copy number variation1nstd214human GRCh38 chr7: 87,374,848-87,374,930 , GRCh37.p13 chr7: 87,004,164-87,004,246 CROT
    nsv6136273copy number variation1nstd213human GRCh37 chr7: 86,700,000-87,470,001 , GRCh38.p12 chr7: 87,070,684-87,840,686 ABCB1, CROT, 9 more genes
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
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