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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098440copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,036,445-140,138,008 , GRCh38.p12 chr9: 137,141,993-137,243,556 SSNA1, CYSRT1, 14 more genes
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7097938copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 140,040,158-141,016,451 , GRCh38.p12 chr9: 137,145,706-138,121,999 NELFB, LOC651337, 39 more genes
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv6897650copy number variation1nstd229human GRCh38 chr9: 137,167,601-137,169,600 , GRCh37.p13 chr9: 140,062,053-140,064,052 TMEM210, LRRC26, 2 more genes
    nsv6879141copy number variation1nstd229human GRCh38 chr9: 137,145,000-137,226,807 , GRCh37.p13 chr9: 140,039,452-140,121,259 LOC105376328, NDOR1, 11 more genes
    nsv6633592copy number variation2nstd224human GRCh37 chr9: 140,063,557-140,108,448 , GRCh38.p12 chr9: 137,169,105-137,213,996 GRIN1, SSNA1, 7 more genes
    nsv6633162copy number variation1nstd224human GRCh37 chr9: 140,054,136-140,069,828 , GRCh38.p12 chr9: 137,159,684-137,175,376 GRIN1, ANAPC2, 3 more genes
    nsv6450572copy number variation1nstd223human GRCh38 chr9: 135,800,101-137,359,000 , GRCh37.p13 chr9: 138,691,947-140,253,452 LCN6, PAXX, 96 more genes
    nsv6448504copy number variation1nstd223human GRCh38 chr9: 135,900,001-137,301,100 , GRCh37.p13 chr9: 138,791,847-140,195,552 DIPK1B, LOC105376326, 95 more genes
    nsv6313986copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,563,039-140,310,033 , GRCh38.p12 chr9: 136,668,587-137,415,581 RABL6, ANAPC2, 68 more genes
    nsv6313935copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937 ENTR1, LINC02692, 115 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
    nsv6267241copy number variation1nstd214human GRCh38 chr9: 137,170,869-137,170,938 , GRCh37.p13 chr9: 140,065,321-140,065,390 TMEM210
    nsv6137446copy number variation1nstd213human GRCh37 chr9: 138,580,000-141,150,001 , GRCh38.p12 chr9: 135,688,154-138,259,551 ABCA2, C8G, 123 more genes
    nsv6137065copy number variation1nstd213human GRCh37 chr9: 140,000,000-140,280,001 , GRCh38.p12 chr9: 137,105,548-137,385,549 GRIN1, MAN1B1, 22 more genes
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