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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 more genes
    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
    nsv6454773copy number variation1nstd223human GRCh38 chr9: 62,896,801-62,929,400 , GRCh37.p13 chr9: 66,552,625-66,585,224 CNTNAP3P1, FAM88B, 1 more genes
    nsv6438710copy number variation1nstd223human GRCh38 chr9: 62,821,301-62,922,700 , GRCh37.p13 chr9: 66,477,125-66,578,524 PTGER4P2, FAM88B, 7 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
    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
    nsv6085334insertion1nstd212human GRCh38 chr9: 62,877,691-62,877,691 , GRCh37.p13 chr9: 66,533,515-66,533,515 LERFS
    nsv6019495copy number variation1nstd212human GRCh38 chr9: 62,876,633-62,877,497 , GRCh37.p13 chr9: 66,532,457-66,533,321 LERFS
    nsv6011152copy number variation1nstd212human GRCh38 chr9: 62,889,733-62,889,881 , GRCh37.p13 chr9: 66,545,557-66,545,705 FGF7P8, LERFS
    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
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