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Items: 1 to 20 of 199

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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
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5972210inversion1nstd209human GRCh38 chr9: 36,238,245-37,822,315 , GRCh37.p13 chr9: 36,238,242-37,822,312 PAX5, GRHPR, 35 more genes
    nsv5911566copy number variation1nstd209human GRCh38 chr9: 37,090,844-37,096,020 , GRCh37.p13 chr9: 37,090,841-37,096,017 EBLN3P
    nsv5638609insertion1nstd207human GRCh38 chr9: 37,086,919-37,086,919 , GRCh37.p13 chr9: 37,086,916-37,086,916 EBLN3P
    nsv5492057copy number variation1nstd206human GRCh38 chr9: 37,090,816-37,096,031 , GRCh37.p13 chr9: 37,090,813-37,096,028 EBLN3P
    nsv5483734copy number variation1nstd206human GRCh38 chr9: 37,056,000-37,102,000 , GRCh37.p13 chr9: 37,055,997-37,101,997 EBLN3P
    nsv5241146copy number variation1nstd204human GRCh38.p13 chr9: 37,073,644-37,106,507 , GRCh37.p13 chr9: 37,073,641-37,106,504 EBLN3P
    nsv4964382copy number variation1nstd200human GRCh38 chr9: 37,078,405-37,079,183 , GRCh37.p13 chr9: 37,078,402-37,079,180 EBLN3P
    nsv4828308copy number variation1nstd200human GRCh37 chr9: 37,078,402-37,079,180 , GRCh38.p12 chr9: 37,078,405-37,079,183 EBLN3P
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675481copy number variation1nstd102humanUncertain significance GRCh37 chr9: 36,539,229-38,787,480 , GRCh38.p12 chr9: 36,539,232-38,787,483 LOC105376042, CYP4F33P, 54 more genes
    nsv4611154copy number variation1nstd183human GRCh37 chr9: 37,050,148-37,092,433 , GRCh38.p12 chr9: 37,050,151-37,092,436 EBLN3P
    nsv4606271copy number variation1nstd183human GRCh37 chr9: 37,086,996-37,108,986 , GRCh38.p12 chr9: 37,086,999-37,108,989 EBLN3P, LOC105376034
    nsv4605030copy number variation1nstd183human GRCh37 chr9: 37,075,997-37,108,986 , GRCh38.p12 chr9: 37,076,000-37,108,989 LOC105376034, EBLN3P
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