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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7073548inversion1nstd229human GRCh38 chr17: 30,822,062-31,121,129 , GRCh37.p13 chr17: 29,149,080-29,448,147 MIR4733HG, NF1, 12 more genes
    nsv7063502inversion1nstd229human GRCh38 chr17: 30,624,449-32,040,578 , GRCh37.p13 chr17: 28,951,467-30,367,597 ATAD5, SH3GL1P2, 42 more genes
    nsv7063155inversion1nstd229human GRCh38 chr17: 30,625,646-31,100,945 , GRCh37.p13 chr17: 28,952,664-29,427,963 MIR4733, CRLF3, 19 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7059883inversion1nstd229human GRCh38 chr17: 30,955,570-30,995,042 , GRCh37.p13 chr17: 29,282,588-29,322,060 ADAP2, RN7SL138P, 2 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
    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
    nsv6980000copy number variation1nstd229human GRCh38 chr17: 30,478,656-31,031,751 , GRCh37.p13 chr17: 28,805,674-29,358,769 LOC100420850, SH3GL1P2, 22 more genes
    nsv6979393copy number variation1nstd229human GRCh38 chr17: 30,886,472-30,977,371 , GRCh37.p13 chr17: 29,213,490-29,304,389 ADAP2, ATAD5, 4 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
    nsv6624068copy number variation1nstd224human GRCh37 chr17: 29,000,019-29,326,155 , GRCh38.p12 chr17: 30,673,001-30,999,137 RN7SL316P, CRLF3, 10 more genes
    nsv6584877inversion1nstd223human GRCh38 chr17: 30,625,643-31,100,945 , GRCh37.p13 chr17: 28,952,661-29,427,963 SH3GL1P2, LOC100420850, 19 more genes
    nsv6502359copy number variation1nstd223human GRCh38 chr17: 30,976,263-30,977,566 , GRCh37.p13 chr17: 29,303,281-29,304,584 DPRXP4, RNF135
    nsv6499938copy number variation1nstd223human GRCh38 chr17: 30,972,146-31,005,786 , GRCh37.p13 chr17: 29,299,164-29,332,804 LOC107984974, RNF135, 1 more genes
    nsv6314760inversion1nstd102humanPathogenic GRCh37.p13 chr17: 28,987,626-29,486,186 , GRCh38 chr17: 30,660,608-31,159,168 NF1, CRLF3, 15 more genes
    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
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