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Items: 1 to 20 of 959

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7146482insertion1nstd232human GRCh37.p13 chr1: 241,466,354-241,466,354 , GRCh38.p12 chr1: 241,303,054-241,303,054 RGS7
    nsv7140259copy number variation1nstd232human GRCh37.p13 chr1: 241,186,304-241,186,426 , GRCh38.p12 chr1: 241,023,004-241,023,126 RGS7
    nsv7099270copy number variation1nstd231human GRCh38.p12 chr1: 237,610,040-242,246,069 , GRCh37 chr1: 237,773,340-242,409,371 CHML, CHRM3, 59 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7057866inversion1nstd229human GRCh38 chr1: 241,146,879-241,150,419 , GRCh37.p13 chr1: 241,310,179-241,313,719 RGS7
    nsv7053794inversion1nstd229human GRCh38 chr1: 240,953,796-240,958,332 , GRCh37.p13 chr1: 241,117,096-241,121,632 RGS7
    nsv7050815inversion1nstd229human GRCh38 chr1: 240,664,933-241,655,110 , GRCh37.p13 chr1: 240,828,233-241,818,412 THAP12P8, OPN3, 12 more genes
    nsv7048996inversion1nstd229human GRCh38 chr1: 240,958,080-240,963,930 , GRCh37.p13 chr1: 241,121,380-241,127,230 RGS7
    nsv7048087inversion1nstd229human GRCh38 chr1: 240,132,685-242,030,818 , GRCh37.p13 chr1: 240,295,985-242,194,120 RPS11P2, MIR3123, 27 more genes
    nsv7046612inversion1nstd229human GRCh38 chr1: 240,895,461-240,898,515 , GRCh37.p13 chr1: 241,058,761-241,061,815 RGS7
    nsv7045904inversion1nstd229human GRCh38 chr1: 236,415,671-241,161,975 , GRCh37.p13 chr1: 236,578,971-241,325,275 PSMD2P1, RN7SKP195, 55 more genes
    nsv7042931inversion1nstd229human GRCh38 chr1: 240,957,698-240,957,771 , GRCh37.p13 chr1: 241,120,998-241,121,071 RGS7
    nsv7042632inversion1nstd229human GRCh38 chr1: 238,193,966-241,052,503 , GRCh37.p13 chr1: 238,357,266-241,215,803 LOC105373222, FMN2, 27 more genes
    nsv7042287inversion1nstd229human GRCh38 chr1: 241,142,633-241,147,348 , GRCh37.p13 chr1: 241,305,933-241,310,648 RGS7
    nsv7040493inversion1nstd229human GRCh38 chr1: 240,436,239-242,512,823 , GRCh37.p13 chr1: 240,599,539-242,676,125 CFL1P4, RNU5F-8P, 34 more genes
    nsv7038410inversion1nstd229human GRCh38 chr1: 240,665,018-241,655,164 , GRCh37.p13 chr1: 240,828,318-241,818,466 LOC100506929, MIR3123, 12 more genes
    nsv6678037copy number variation1nstd229human GRCh38 chr1: 240,840,537-240,842,694 , GRCh37.p13 chr1: 241,003,837-241,005,994 RGS7
    nsv6677858copy number variation1nstd229human GRCh38 chr1: 241,244,370-241,250,138 , GRCh37.p13 chr1: 241,407,670-241,413,438 RGS7
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