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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097677copy number variation1nstd102humanPathogenic GRCh37 chr9: 104,124,710-104,500,261 , GRCh38.p12 chr9: 101,362,428-101,737,979 TMEM246-AS1, PGAP4, 10 more genes
    nsv6877591copy number variation1nstd229human GRCh38 chr9: 101,373,218-101,377,229 , GRCh37.p13 chr9: 104,135,500-104,139,511 BAAT, FYTTD1P1
    nsv6877464copy number variation1nstd229human GRCh38 chr9: 101,348,970-101,358,618 , GRCh37.p13 chr9: 104,111,252-104,120,900 TRMT112P4, LOC100421197, 1 more genes
    nsv6868418copy number variation1nstd229human GRCh38 chr9: 101,302,335-101,603,079 , GRCh37.p13 chr9: 104,064,617-104,365,361 RNF20, PLPPR1, 14 more genes
    nsv6860847copy number variation1nstd229human GRCh38 chr9: 101,381,727-101,381,887 , GRCh37.p13 chr9: 104,144,009-104,144,169 BAAT
    nsv6859938copy number variation1nstd229human GRCh38 chr9: 101,373,001-101,381,200 , GRCh37.p13 chr9: 104,135,283-104,143,482 BAAT, FYTTD1P1
    nsv6858150copy number variation1nstd229human GRCh38 chr9: 101,319,338-101,389,524 , GRCh37.p13 chr9: 104,081,620-104,151,806 LOC100421197, ACNATP, 5 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
    nsv6453547copy number variation1nstd223human GRCh38 chr9: 101,370,666-101,371,320 , GRCh37.p13 chr9: 104,132,948-104,133,602 BAAT, FYTTD1P1
    nsv6451969copy number variation1nstd223human GRCh38 chr9: 101,372,617-101,373,068 , GRCh37.p13 chr9: 104,134,899-104,135,350 FYTTD1P1, BAAT
    nsv6442102copy number variation1nstd223human GRCh38 chr9: 101,367,627-101,370,483 , GRCh37.p13 chr9: 104,129,909-104,132,765 BAAT
    nsv6436544copy number variation1nstd223human GRCh38 chr9: 101,367,148-101,367,776 , GRCh37.p13 chr9: 104,129,430-104,130,058 BAAT
    nsv6435729copy number variation1nstd223human GRCh38 chr9: 101,362,667-101,363,106 , GRCh37.p13 chr9: 104,124,949-104,125,388 BAAT
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6136627copy number variation1nstd213human GRCh37 chr9: 104,030,000-104,350,001 , GRCh38.p12 chr9: 101,267,718-101,587,719 ALDOB, BAAT, 12 more genes
    nsv6099605insertion1nstd212human GRCh38 chr9: 101,358,928-101,358,928 , GRCh37.p13 chr9: 104,121,210-104,121,210 LOC100421197, BAAT
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