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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063502inversion1nstd229human GRCh38 chr17: 30,624,449-32,040,578 , GRCh37.p13 chr17: 28,951,467-30,367,597 ATAD5, SH3GL1P2, 42 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6991213copy number variation1nstd229human GRCh38 chr17: 31,560,039-31,562,810 , GRCh37.p13 chr17: 29,887,058-29,889,829 MIR193A, RNU6ATAC7P
    nsv6987354copy number variation1nstd229human GRCh38 chr17: 30,757,760-31,964,420 , GRCh37.p13 chr17: 29,084,778-30,291,439 EVI2A, OMG, 34 more genes
    nsv6982533copy number variation1nstd229human GRCh38 chr17: 30,657,528-32,073,539 , GRCh37.p13 chr17: 28,984,546-30,400,558 UTP6, LOC107984974, 38 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6634407copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,076,232-30,043,725 , GRCh38.p12 chr17: 30,749,214-31,716,706 RAB11FIP4, RNU6-1134P, 29 more genes
    nsv6505996copy number variation1nstd223human GRCh38 chr17: 31,555,979-31,560,380 , GRCh37.p13 chr17: 29,882,998-29,887,399 MIR193A
    nsv6290215copy number variation1nstd102humanPathogenic GRCh37 chr17: 28,992,701-30,408,700 , GRCh38.p12 chr17: 30,665,683-32,081,681 MIR4733, RN7SL138P, 38 more genes
    nsv6133299copy number variation1nstd213human GRCh37 chr17: 28,940,000-30,220,001 , GRCh38.p12 chr17: 30,612,982-31,892,982 AK4P1, EVI2A, 39 more genes
    nsv6133237copy number variation1nstd213human GRCh37 chr17: 29,820,000-29,960,001 , GRCh38.p12 chr17: 31,492,982-31,632,982 RAB11FIP4, MIR193A, 6 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6105514inversion1nstd212human GRCh38 chr17: 30,625,589-32,037,972 , GRCh37.p13 chr17: 28,952,607-30,364,991 AK4P1, EVI2A, 41 more genes
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5016007copy number variation1nstd200human GRCh38 chr17: 31,557,605-31,559,132 , GRCh37.p13 chr17: 29,884,624-29,886,151 MIR193A
    nsv5016006copy number variation1nstd200human GRCh38 chr17: 31,555,979-31,560,380 , GRCh37.p13 chr17: 29,882,998-29,887,399 MIR193A
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4684241copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,393,104-30,427,403 , GRCh38.p12 chr17: 31,066,086-32,100,384 LOC102724625, RNA5SP437, 26 more genes
    nsv4680260copy number variation1nstd189human GRCh37.p13 chr17: 29,540,484-30,103,257 , GRCh38.p12 chr17: 31,213,466-31,776,238 AK4P1, EVI2A, 16 more genes
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