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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
    nsv5954432insertion1nstd209human GRCh38 chr9: 62,884,995-62,884,995 , GRCh37.p13 chr9: 66,540,819-66,540,819 LERFS
    nsv5949180insertion1nstd209human GRCh38 chr9: 62,864,463-62,864,463 , GRCh37.p13 chr9: 66,520,287-66,520,287 LERFS
    nsv5920869copy number variation1nstd209human GRCh38 chr9: 62,876,615-62,877,480 , GRCh37.p13 chr9: 66,532,439-66,533,304 LERFS
    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
    nsv5665110inversion1nstd207human GRCh38 chr9: 62,873,694-62,937,603 , GRCh37.p13 chr9: 66,529,518-66,593,427 LERFS, FAM88B, 2 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
    nsv5491060copy number variation1nstd206human GRCh38 chr9: 62,876,615-62,877,497 , GRCh37.p13 chr9: 66,532,439-66,533,321 LERFS
    nsv5479197copy number variation1nstd206human GRCh38 chr9: 62,868,078-62,871,040 , GRCh37.p13 chr9: 66,523,902-66,526,864 LERFS
    nsv5430793copy number variation1nstd206human GRCh38 chr9: 62,834,950-62,896,832 , GRCh37.p13 chr9: 66,490,774-66,552,656 PTGER4P2, ADGRF5P1, 7 more genes
    nsv5386733copy number variation1nstd186human GRCh37 chr9: 66,532,439-66,533,321 , GRCh38.p12 chr9: 62,876,615-62,877,497 LERFS
    nsv5386638copy number variation1nstd186human GRCh37 chr9: 66,532,444-66,533,321 , GRCh38.p12 chr9: 62,876,620-62,877,497 LERFS
    nsv5316518copy number variation1nstd204human GRCh38.p13 chr9: 62,876,614-62,877,497 , GRCh37.p13 chr9: 66,532,438-66,533,321 LERFS
    nsv5312596copy number variation1nstd204human GRCh38.p13 chr9: 62,868,090-62,871,059 , GRCh37.p13 chr9: 66,523,914-66,526,883 LERFS
    nsv5259623copy number variation1nstd204human GRCh38.p13 chr9: 62,849,101-62,888,300 , GRCh37.p13 chr9: 66,504,925-66,544,124 LERFS, MYO5BP2, 2 more genes
    nsv5258781copy number variation1nstd204human GRCh38.p13 chr9: 62,848,901-62,886,800 , GRCh37.p13 chr9: 66,504,725-66,542,624 MYO5BP2, FGF7P8, 2 more genes
    nsv5257844copy number variation1nstd204human GRCh38.p13 chr9: 62,860,101-62,875,400 , GRCh37.p13 chr9: 66,515,925-66,531,224 ADGRF5P1, LERFS
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