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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876635copy number variation1nstd229human GRCh38 chr9: 72,384,161-74,793,192 , GRCh37.p13 chr9: 74,999,077-77,408,108 LOC101927329, LOC100289351, 27 more genes
    nsv6873671copy number variation1nstd229human GRCh38 chr9: 73,407,001-74,070,600 , GRCh37.p13 chr9: 76,021,917-76,685,516 LOC105376084, DPP3P2, 6 more genes
    nsv6858263copy number variation1nstd229human GRCh38 chr9: 72,621,927-73,648,904 , GRCh37.p13 chr9: 75,236,843-76,263,820 RPS20P24, LINC01474, 13 more genes
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633478copy number variation1nstd224human GRCh37 chr9: 76,242,155-76,767,313 , GRCh38.p12 chr9: 73,627,239-74,152,397 LOC101927329, LOC105376086, 3 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6137094copy number variation1nstd213human GRCh37 chr9: 71,840,000-78,800,001 , GRCh38.p12 chr9: 69,225,084-76,185,085 KLF9, PCSK5, 83 more genes
    nsv4968401copy number variation1nstd200human GRCh38 chr9: 73,641,265-73,647,131 , GRCh37.p13 chr9: 76,256,181-76,262,047 LOC100422376
    nsv4814074copy number variation1nstd200human GRCh37 chr9: 76,256,181-76,262,047 , GRCh38.p12 chr9: 73,641,265-73,647,131 LOC100422376
    nsv4611134copy number variation1nstd183human GRCh37 chr9: 76,254,216-76,262,399 , GRCh38.p12 chr9: 73,639,300-73,647,483 LOC100422376
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv3923526copy number variation1nstd102humanPathogenic NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127 GCNT1, NMRK1, 65 more genes
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