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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066246inversion1nstd229human GRCh38 chr9: 61,567,441-63,740,704 , GRCh37.p13 chr: NaN-NaN FGF7P6, LOC105379807, 47 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
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 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
    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
    nsv6142842copy number variation1nstd206human GRCh38 chr9: 61,785,368-61,976,000 , GRCh37.p13 chr9: 44,960,294-45,697,082 , FAM27C, 7 more genes
    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
    nsv5975553inversion1nstd209human GRCh38 chr9: 61,533,844-61,993,067 , GRCh37.p13 chr9: 44,741,682-45,697,082 , FAM27C, 9 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
    nsv5584617copy number variation1nstd207human GRCh38 chr9: 61,855,360-61,857,070 , GRCh37.p13 chr9: 44,991,512-44,993,222 FAM27C, FAM27E4
    nsv5554508sequence alteration1nstd206human GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104 , PTGER4P2, 168 more genes
    nsv5245023copy number variation1nstd204human GRCh38.p13 chr9: 61,850,601-61,853,400 , GRCh37.p13 chr9: 44,986,753-44,989,552 FAM27C
    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
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
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