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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456425copy number variation1nstd102humanUncertain significance GRCh37 chr6: 112,352,198-112,457,238 , GRCh38.p12 chr6: 112,030,995-112,136,036 TUBE1, CCN6, 3 more genes
    nsv3880626copy number variation1nstd102humanPathogenic GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541 TUBE1, LOC107986534, 426 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 TUBE1, RN7SL509P, 311 more genes
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3920683copy number variation1nstd102humanPathogenic NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720 TUBE1, SSXP10, 298 more genes
    nsv3876958copy number variation1nstd102humanPathogenic GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766 TUBE1, LIN28B-AS1, 258 more genes
    nsv3910417copy number variation1nstd102humanPathogenic GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300 TUBE1, LINC02518, 266 more genes
    nsv3924741copy number variation1nstd102humanPathogenic GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058 TUBE1, LOC105377979, 266 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 TUBE1, LOC101927405, 211 more genes
    nsv3919897copy number variation1nstd102humanPathogenic NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239 TUBE1, HACE1, 174 more genes
    nsv4457007copy number variation1nstd102humanPathogenic GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231 TUBE1, HDAC2-AS2, 134 more genes
    nsv3914025copy number variation1nstd102humanPathogenic NCBI36 chr6: 107,798,038-116,255,339 , GRCh38 chr6: 107,370,141-115,827,482 , GRCh37 chr6: 107,691,345-116,148,646 TUBE1, TRAF3IP2-AS1, 139 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 TUBE1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 TUBE1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 TUBE1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 TUBE1, ITPR3, 2905 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 TUBE1, RNU6-770P, 810 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 TUBE1, RPL23AP50, 216 more genes
    nsv3906984copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,069,445-120,994,664 , GRCh38.p12 chr6: 111,748,242-120,673,518 TUBE1, COL10A1, 115 more genes
    nsv3913432copy number variation1nstd102humanUncertain significance NCBI36 chr6: 112,438,811-112,672,113 , GRCh37 chr6: 112,332,118-112,565,420 , GRCh38 chr6: 112,010,915-112,244,218 TUBE1, LAMA4, 5 more genes
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