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Items: 1 to 20 of 277

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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
    nsv5259323copy number variation1nstd204human GRCh38.p13 chr9: 62,371,001-62,422,700 , GRCh37.p13 chr9: 46,682,302-46,734,001 FAM88C, FGF7P6
    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
    nsv5258207copy number variation1nstd204human GRCh38.p13 chr9: 62,376,801-62,381,400 , GRCh37.p13 chr9: 46,688,102-46,692,701 FGF7P6, FAM88C
    nsv5256415copy number variation1nstd204human GRCh38.p13 chr9: 62,373,001-62,377,300 , GRCh37.p13 chr9: 46,684,302-46,688,601 FGF7P6, FAM88C
    nsv5255572copy number variation1nstd204human GRCh38.p13 chr9: 62,373,101-62,396,100 , GRCh37.p13 chr9: 46,684,402-46,707,401 FAM88C, FGF7P6
    nsv5249899copy number variation1nstd204human GRCh38.p13 chr9: 62,370,301-62,381,700 , GRCh37.p13 chr9: 46,681,602-46,693,001 FAM88C, FGF7P6
    nsv5249356copy number variation1nstd204human GRCh38.p13 chr9: 62,370,301-62,385,600 , GRCh37.p13 chr9: 46,681,602-46,696,901 FGF7P6, FAM88C
    nsv5248681copy number variation1nstd204human GRCh38.p13 chr9: 62,370,301-62,372,700 , GRCh37.p13 chr9: 46,681,602-46,684,001 FAM88C
    nsv5247628copy number variation1nstd204human GRCh38.p13 chr9: 62,372,901-62,384,600 , GRCh37.p13 chr9: 46,684,202-46,695,901 FAM88C, FGF7P6
    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
    nsv5243264copy number variation1nstd204human GRCh38.p13 chr9: 62,364,501-62,384,800 , GRCh37.p13 chr9: 46,675,802-46,696,101 FGF7P6, FAM88C
    nsv5242433copy number variation1nstd204human GRCh38.p13 chr9: 62,373,601-62,374,500 , GRCh37.p13 chr9: 46,684,902-46,685,801 FGF7P6, FAM88C
    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
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