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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054819inversion1nstd229human GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354 SRP19, LINCADL, 53 more genes
    nsv6776358copy number variation1nstd229human GRCh38 chr5: 115,325,901-115,510,700 , GRCh37.p13 chr5: 114,661,598-114,846,397 LOC105379130, CCT5P1, 4 more genes
    nsv6773484copy number variation1nstd229human GRCh38 chr5: 115,390,962-115,393,489 , GRCh37.p13 chr5: 114,726,659-114,729,186 CTNNA1P1, LOC105379130
    nsv6765113copy number variation1nstd229human GRCh38 chr5: 115,335,676-115,452,084 , GRCh37.p13 chr5: 114,671,373-114,787,781 CTNNA1P1, AK3P4, 2 more genes
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6630082copy number variation1nstd224human GRCh37 chr5: 114,279,914-116,657,759 , GRCh38.p12 chr5: 114,944,217-117,322,063 LVRN, TICAM2, 44 more genes
    nsv6409047copy number variation1nstd223human GRCh38 chr5: 115,331,801-115,399,900 , GRCh37.p13 chr5: 114,667,498-114,735,597 LOC105379130, LOC105379129, 1 more genes
    nsv6403265copy number variation1nstd223human GRCh38 chr5: 115,390,961-115,393,488 , GRCh37.p13 chr5: 114,726,658-114,729,185 LOC105379130, CTNNA1P1
    nsv6313698copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,443,783-116,255,660 , GRCh38.p12 chr5: 112,108,086-116,919,964 RPS17P2, COMMD10, 71 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6135639copy number variation1nstd213human GRCh37 chr5: 113,920,000-120,810,001 , GRCh38.p12 chr5: 114,584,303-121,474,306 CDO1, AP3S1, 83 more genes
    nsv6135376copy number variation1nstd213human GRCh37 chr5: 114,660,000-114,950,001 , GRCh38.p12 chr5: 115,324,303-115,614,304 TICAM2, TICAM2-AS1, 9 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5972434inversion1nstd209human GRCh37.p13 chr5: 114,252,584-114,781,685 , GRCh38 chr5: 114,916,887-115,445,988 CTNNA1P1, PGGT1B, 7 more genes
    nsv5454800copy number variation1nstd206human GRCh38 chr5: 115,390,961-115,393,488 , GRCh37.p13 chr5: 114,726,658-114,729,185 LOC105379130, CTNNA1P1
    nsv5368844translocation1nstd200human GRCh38 chr5: 115,390,961-115,390,961 , GRCh38 chr5: 115,393,488-115,393,488 , GRCh37.p13 chr5: 114,726,658-114,726,658 , GRCh37.p13 chr5: 114,729,185-114,729,185 LOC105379130, CTNNA1P1
    nsv5337016translocation1nstd200human GRCh37 chr5: 114,726,658-114,726,658 , GRCh37 chr5: 114,729,185-114,729,185 , GRCh38.p12 chr5: 115,390,961-115,390,961 , GRCh38.p12 chr5: 115,393,488-115,393,488 LOC105379130, CTNNA1P1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
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