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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095730copy number variation1nstd102humanUncertain significance GRCh37 chr19: 852,329-855,814 , GRCh38.p12 chr19: 852,329-855,814 , GRCh38.p12 chr19|NT_187622.1: 31,216-34,700 ELANE
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7073159inversion1nstd229human GRCh38 chr19: 249,047-1,189,238 , GRCh37.p13 chr19: 249,047-1,189,237 MADCAM1-AS1, ARID3A, 53 more genes
    nsv7064913inversion1nstd229human GRCh38 chr19: 558,352-1,188,612 , GRCh37.p13 chr19: 558,352-1,188,611 MIR4745, R3HDM4, 40 more genes
    nsv7005342copy number variation1nstd229human GRCh38 chr19: 855,455-859,952 , GRCh37.p13 chr19: 855,455-859,952 CFD, ELANE
    nsv7004542copy number variation1nstd229human GRCh38 chr19: 850,140-854,266 , GRCh37.p13 chr19: 850,140-854,266 ELANE
    nsv7001057copy number variation1nstd229human GRCh38 chr19: 856,384-865,338 , GRCh37.p13 chr19: 856,384-865,338 CFD, ELANE
    nsv6998478copy number variation1nstd229human GRCh38 chr19: 842,913-852,644 , GRCh37.p13 chr19: 842,913-852,644 ELANE, PRTN3
    nsv6625515copy number variation1nstd224human GRCh37 chr19: 856,015-891,008 , GRCh38.p12 chr19: 856,015-891,008 , GRCh38.p12 chr19|NT_187622.1: 34,901-61,733 ELANE, MED16, 1 more genes
    nsv6625514copy number variation1nstd224human GRCh37 chr19: 844,020-859,374 , GRCh38.p12 chr19: 844,020-859,374 , GRCh38.p12 chr19|NT_187622.1: 22,863-38,254 ELANE, PRTN3, 1 more genes
    nsv6625463copy number variation1nstd224human GRCh37 chr19: 841,398-891,119 , GRCh38.p12 chr19: 841,398-891,119 , GRCh38.p12 chr19|NT_187622.1: 20,241-61,733 MED16, CFD, 2 more genes
    nsv6625461copy number variation1nstd224human GRCh37 chr19: 765,568-945,710 , GRCh38.p12 chr19: 765,568-945,710 ARID3A, PRTN3, 13 more genes
    nsv6625065copy number variation1nstd224human GRCh37 chr19: 839,158-850,023 , GRCh38.p12 chr19: 839,158-850,023 , GRCh38.p12 chr19|NT_187622.1: 18,001-28,858 ELANE, PRTN3
    nsv6625064copy number variation1nstd224human GRCh37 chr19: 815,834-929,895 , GRCh38.p12 chr19: 815,834-929,895 , GRCh38.p12 chr19|NT_187622.1: 1-61,733 ARID3A, PRTN3, 8 more genes
    nsv6597832inversion1nstd223human GRCh38 chr19: 558,351-1,188,654 , GRCh37.p13 chr19: 558,351-1,188,653 HCN2, TMEM259, 40 more genes
    nsv6535444copy number variation1nstd223human GRCh38 chr19: 832,934-858,008 , GRCh37.p13 chr19: 832,934-858,008 PRTN3, CFD, 1 more genes
    nsv6524787copy number variation1nstd223human GRCh38 chr19: 840,133-915,536 , GRCh37.p13 chr19: 840,133-915,536 KISS1R, ELANE, 5 more genes
    nsv6523907copy number variation1nstd223human GRCh38 chr19: 854,684-855,054 , GRCh37.p13 chr19: 854,684-855,054 ELANE
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