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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
    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
    nsv5259164copy number variation1nstd204human GRCh38.p13 chr9: 64,708,001-64,710,300 , GRCh37.p13 chr9: 69,720,419-69,722,718 BMS1P11
    nsv5245730copy number variation1nstd204human GRCh38.p13 chr9: 64,704,401-64,706,400 , GRCh37.p13 chr9: 69,716,819-69,718,818 BMS1P11
    nsv5243434copy number variation1nstd204human GRCh38.p13 chr9: 64,701,001-64,707,200 , GRCh37.p13 chr9: 69,713,419-69,719,618 BMS1P11
    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
    nsv4730150inversion32nstd198human GRCh38 chr9: 63,409,844-65,048,344 , GRCh37.p13 chr9: 42,744,224-45,643,649 , GRCh37.p13 chr9: 67,364,816-70,010,542 , IGKV1OR-2, 39 more genes
    nsv4680877copy number variation1nstd189human GRCh37.p13 chr9: 43,635,114-66,323,059 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4680653copy number variation1nstd189human GRCh37.p13 chr9: 45,054,941-69,978,022 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4680342copy number variation1nstd189human GRCh37.p13 chr9: 43,315,671-65,672,607 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 more genes
    nsv4679716copy number variation1nstd189human GRCh37.p13 chr9: 44,114,873-69,844,813 , GRCh38.p12 chr9: 40,711,180-67,920,552 , RBPJP2, 243 more genes
    nsv4679421copy number variation1nstd189human GRCh37.p13 chr9: 44,114,873-67,360,687 , GRCh38.p12 chr9: 41,747,162-65,568,548 , IGKV1OR-2, 153 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
    nsv4673727copy number variation1nstd186human GRCh37 chr9: 38,997,411-46,584,047 , GRCh38.p12 chr9: 40,529,065-67,217,006 , LOC101929878, 232 more genes
    nsv4669248copy number variation1nstd186human GRCh37 chr9: 69,425,058-69,821,850 , GRCh38.p12 chr9: 64,412,640-64,809,432 SNX18P9, CYP4F25P, 15 more genes
    nsv4613257copy number variation2nstd183human GRCh37 chr9: 69,425,058-69,821,850 , GRCh38.p12 chr9: 64,412,640-64,809,432 CYP4F25P, SNX18P9, 15 more genes
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