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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
    nsv7072380inversion1nstd229human GRCh38 chr12: 50,969,371-50,972,888 , GRCh37.p13 chr12: 51,363,154-51,366,671 SLC11A2, HIGD1C
    nsv7063378inversion1nstd229human GRCh38 chr12: 50,912,523-51,136,937 , GRCh37.p13 chr12: 51,306,306-51,530,720 RPL35AP29, CSRNP2, 9 more genes
    nsv7059430inversion1nstd229human GRCh38 chr12: 50,917,961-51,167,647 , GRCh37.p13 chr12: 51,311,744-51,561,430 TMT1A, RPL35AP29, 10 more genes
    nsv6933920copy number variation1nstd229human GRCh38 chr12: 50,947,115-50,973,095 , GRCh37.p13 chr12: 51,340,898-51,366,878 HIGD1C, SLC11A2
    nsv6933701copy number variation1nstd229human GRCh38 chr12: 50,941,937-50,950,553 , GRCh37.p13 chr12: 51,335,720-51,344,336 HIGD1C, SLC11A2
    nsv6932873copy number variation1nstd229human GRCh38 chr12: 50,932,617-50,934,359 , GRCh37.p13 chr12: 51,326,400-51,328,142 TMT1A, HIGD1C
    nsv6931283copy number variation1nstd229human GRCh38 chr12: 50,937,929-50,940,241 , GRCh37.p13 chr12: 51,331,712-51,334,024 HIGD1C
    nsv6930173copy number variation1nstd229human GRCh38 chr12: 50,820,901-51,598,500 , GRCh37.p13 chr12: 51,214,684-51,992,284 RN7SL519P, RNU6-87P, 23 more genes
    nsv6928651copy number variation1nstd229human GRCh38 chr12: 50,932,712-50,941,783 , GRCh37.p13 chr12: 51,326,495-51,335,566 TMT1A, HIGD1C
    nsv6926666copy number variation1nstd229human GRCh38 chr12: 50,954,693-50,982,595 , GRCh37.p13 chr12: 51,348,476-51,376,378 HIGD1C, SLC11A2
    nsv6925776copy number variation1nstd229human GRCh38 chr12: 50,940,401-50,950,500 , GRCh37.p13 chr12: 51,334,184-51,344,283 HIGD1C, SLC11A2
    nsv6921421copy number variation1nstd229human GRCh38 chr12: 50,941,901-50,950,600 , GRCh37.p13 chr12: 51,335,684-51,344,383 HIGD1C, SLC11A2
    nsv6920373copy number variation1nstd229human GRCh38 chr12: 50,936,601-50,940,700 , GRCh37.p13 chr12: 51,330,384-51,334,483 HIGD1C
    nsv6579351inversion1nstd223human GRCh38 chr12: 50,957,220-50,957,896 , GRCh37.p13 chr12: 51,351,003-51,351,679 HIGD1C, SLC11A2
    nsv6578943inversion1nstd223human GRCh38 chr12: 50,968,537-50,969,548 , GRCh37.p13 chr12: 51,362,320-51,363,331 HIGD1C, SLC11A2
    nsv6577200inversion1nstd223human GRCh38 chr12: 50,950,963-50,951,930 , GRCh37.p13 chr12: 51,344,746-51,345,713 HIGD1C, SLC11A2
    nsv6576852inversion1nstd223human GRCh38 chr12: 50,958,735-50,959,381 , GRCh37.p13 chr12: 51,352,518-51,353,164 HIGD1C, SLC11A2
    nsv6473443copy number variation1nstd223human GRCh38 chr12: 50,968,829-50,972,885 , GRCh37.p13 chr12: 51,362,612-51,366,668 SLC11A2, HIGD1C
    nsv6472699copy number variation1nstd223human GRCh38 chr12: 50,941,952-50,950,535 , GRCh37.p13 chr12: 51,335,735-51,344,318 HIGD1C, SLC11A2
    nsv6306507copy number variation1nstd186human GRCh37 chr12: 51,341,663-51,342,602 , GRCh38.p12 chr12: 50,947,880-50,948,819 HIGD1C
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