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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5554508sequence alteration1nstd206human GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104 , PTGER4P2, 168 more genes
    nsv5258702copy number variation1nstd204human GRCh38.p13 chr9: 62,359,801-62,380,600 , GRCh37.p13 chr9: 46,671,102-46,691,901 RN7SL544P, FGF7P6, 1 more genes
    nsv5258259copy number variation1nstd204human GRCh38.p13 chr9: 62,363,901-62,368,000 , GRCh37.p13 chr9: 46,675,202-46,679,301 RN7SL544P
    nsv5257930copy number variation1nstd204human GRCh38.p13 chr9: 62,265,701-62,362,000 , GRCh37.p13 chr9: 46,577,002-46,673,301 RN7SL544P, LOC105379263, 1 more genes
    nsv5256305copy number variation1nstd204human GRCh38.p13 chr9: 62,350,801-62,366,600 , GRCh37.p13 chr9: 46,662,102-46,677,901 LOC105379263, RN7SL544P
    nsv5251388copy number variation1nstd204human GRCh38.p13 chr9: 62,350,801-62,362,100 , GRCh37.p13 chr9: 46,662,102-46,673,401 LOC105379263, RN7SL544P
    nsv5248298copy number variation1nstd204human GRCh38.p13 chr9: 62,360,101-62,362,100 , GRCh37.p13 chr9: 46,671,402-46,673,401 RN7SL544P
    nsv5247981copy number variation1nstd204human GRCh38.p13 chr9: 62,360,101-62,366,600 , GRCh37.p13 chr9: 46,671,402-46,677,901 RN7SL544P
    nsv5247150copy number variation1nstd204human GRCh38.p13 chr9: 62,357,301-62,362,100 , GRCh37.p13 chr9: 46,668,602-46,673,401 RN7SL544P
    nsv5244616copy number variation1nstd204human GRCh38.p13 chr9: 62,350,801-62,407,300 , GRCh37.p13 chr9: 46,662,102-46,718,601 FAM88C, FGF7P6, 2 more genes
    nsv5242908copy number variation1nstd204human GRCh38.p13 chr9: 62,350,801-62,370,100 , GRCh37.p13 chr9: 46,662,102-46,681,401 LOC105379263, RN7SL544P
    nsv5242301copy number variation1nstd204human GRCh38.p13 chr9: 62,359,801-62,371,100 , GRCh37.p13 chr9: 46,671,102-46,682,401 RN7SL544P
    nsv5242247copy number variation1nstd204human GRCh38.p13 chr9: 62,265,701-62,424,700 , GRCh37.p13 chr9: 46,577,002-46,736,001 RN7SL544P, FGF7P6, 3 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
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