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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096918copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 7,968,276-10,192,634 , GRCh38.p12 chr2: 7,828,145-10,052,507 ITGB1BP1, LINC00299, 37 more genes
    nsv7051196inversion1nstd229human GRCh38 chr2: 9,336,629-9,587,857 , GRCh37.p13 chr2: 9,476,758-9,727,986 ASAP2, ITGB1BP1, 5 more genes
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6665692copy number variation1nstd229human GRCh38 chr2: 9,252,001-9,587,800 , GRCh37.p13 chr2: 9,392,130-9,727,929 ADAM17, ITGB1BP1, 6 more genes
    nsv6661046copy number variation1nstd229human GRCh38 chr2: 9,203,538-9,426,077 , GRCh37.p13 chr2: 9,343,667-9,566,206 ITGB1BP1, CPSF3, 2 more genes
    nsv6658983copy number variation1nstd229human GRCh38 chr2: 9,405,301-9,415,700 , GRCh37.p13 chr2: 9,545,430-9,555,829 ITGB1BP1, ASAP2
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6354580copy number variation1nstd223human GRCh38 chr2: 9,404,804-9,405,367 , GRCh37.p13 chr2: 9,544,933-9,545,496 ITGB1BP1, ASAP2
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6283130insertion1nstd214human GRCh38 chr2: 9,406,008-9,406,008 , GRCh37.p13 chr2: 9,546,137-9,546,137 ASAP2, ITGB1BP1
    nsv6282849insertion1nstd214human GRCh38 chr2: 9,406,010-9,406,010 , GRCh37.p13 chr2: 9,546,139-9,546,139 ASAP2, ITGB1BP1
    nsv6282196insertion1nstd214human GRCh38 chr2: 9,406,561-9,406,561 , GRCh37.p13 chr2: 9,546,690-9,546,690 ITGB1BP1
    nsv6277646insertion1nstd214human GRCh38 chr2: 9,406,007-9,406,007 , GRCh37.p13 chr2: 9,546,136-9,546,136 ITGB1BP1, ASAP2
    nsv6262695copy number variation1nstd214human GRCh38 chr2: 9,406,505-9,406,560 , GRCh37.p13 chr2: 9,546,634-9,546,689 ITGB1BP1
    nsv6262619copy number variation1nstd214human GRCh38 chr2: 9,406,337-9,406,560 , GRCh37.p13 chr2: 9,546,466-9,546,689 ITGB1BP1
    nsv6262618copy number variation1nstd214human GRCh38 chr2: 9,406,031-9,406,086 , GRCh37.p13 chr2: 9,546,160-9,546,215 ITGB1BP1, ASAP2
    nsv6262567copy number variation1nstd214human GRCh38 chr2: 9,406,481-9,406,534 , GRCh37.p13 chr2: 9,546,610-9,546,663 ITGB1BP1
    nsv6262472copy number variation1nstd214human GRCh38 chr2: 9,406,039-9,406,142 , GRCh37.p13 chr2: 9,546,168-9,546,271 ITGB1BP1, ASAP2
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