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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5250040copy number variation1nstd204human GRCh38.p13 chr9: 33,851,001-34,396,200 , GRCh37.p13 chr9: 33,850,999-34,396,198 KIF24, SERPINH1P1, 22 more genes
    nsv5135245mobile element insertion1nstd203human GRCh38 chr9: 34,369,752-34,369,764 , GRCh37.p13 chr9: 34,369,750-34,369,762 MYORG
    nsv4954657copy number variation1nstd200human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 , CCL27, 32 more genes
    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
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4350536copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,309-39,156,958 , GRCh38.p12 chr9: 214,309-39,156,961 CSNK1G2P1, PAICSP1, 576 more genes
    nsv4188495copy number variation1nstd166human GRCh37.p13 chr9: 34,197,962-34,392,075 , GRCh38.p12 chr9: 34,197,964-34,392,077 NUDT2, UBAP1, 7 more genes
    nsv3923714copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-70,630,731 , GRCh37 chr9: 220,253-73,245,647 , NCBI36 chr9: 210,253-72,435,467 LOC105379257, LOC105376002, 888 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921759copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-65,222,364 , GRCh37.p13 chr9: 12,934-65,482,544 , GRCh38.p12 chr9: 12,934-66,233,120 SPATA31A6, CDRT15P14, 824 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3920307copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-38,731,437 , GRCh37 chr9: 204,193-38,741,437 , GRCh38 chr9: 204,193-38,741,440 SIT1, MPDZ, 570 more genes
    nsv3919954copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,861-38,371,639 , GRCh38 chr9: 203,861-38,381,642 , GRCh37 chr9: 203,861-38,381,639 KCNV2, NPR2, 555 more genes
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