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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7061132inversion1nstd229human GRCh38 chr8: 257,097-475,396 , GRCh37.p13 chr8: 207,097-425,396 FBXO25, LOC101927566, 2 more genes
    nsv7060848inversion1nstd229human GRCh38 chr8: 282,167-485,255 , GRCh37.p13 chr8: 232,167-435,255 FBXO25, FAM87A, 1 more genes
    nsv7059572inversion1nstd229human GRCh38 chr8: 310,007-766,676 , GRCh37.p13 chr8: 260,007-716,676 LOC105377773, FBXO25, 5 more genes
    nsv7058829inversion1nstd229human GRCh38 chr8: 299,298-502,102 , GRCh37.p13 chr8: 249,298-452,102 FAM87A, LOC105377773, 2 more genes
    nsv6837769copy number variation1nstd229human GRCh38 chr8: 368,047-489,167 , GRCh37.p13 chr8: 318,047-439,167 FBXO25, TDRP, 1 more genes
    nsv6836779copy number variation1nstd229human GRCh38 chr8: 338,794-437,544 , GRCh37.p13 chr8: 288,794-387,544 FBXO25, FAM87A
    nsv6836740copy number variation1nstd229human GRCh38 chr8: 362,559-381,191 , GRCh37.p13 chr8: 312,559-331,191 FAM87A
    nsv6835887copy number variation1nstd229human GRCh38 chr8: 371,901-485,500 , GRCh37.p13 chr8: 321,901-435,500 FBXO25, FAM87A
    nsv6835231copy number variation1nstd229human GRCh38 chr8: 361,724-384,213 , GRCh37.p13 chr8: 311,724-334,213 FAM87A
    nsv6834434copy number variation1nstd229human GRCh38 chr8: 359,701-382,400 , GRCh37.p13 chr8: 309,701-332,400 FAM87A
    nsv6830881copy number variation1nstd229human GRCh38 chr8: 257,698-400,270 , GRCh37.p13 chr8: 207,698-350,270 LOC105377773, LOC101927566, 1 more genes
    nsv6830762copy number variation1nstd229human GRCh38 chr8: 360,021-456,905 , GRCh37.p13 chr8: 310,021-406,905 FBXO25, FAM87A
    nsv6830414copy number variation1nstd229human GRCh38 chr8: 360,913-382,354 , GRCh37.p13 chr8: 310,913-332,354 FAM87A
    nsv6830346copy number variation1nstd229human GRCh38 chr8: 374,680-378,855 , GRCh37.p13 chr8: 324,680-328,855 FAM87A
    nsv6828421copy number variation1nstd229human GRCh38 chr8: 374,683-378,856 , GRCh37.p13 chr8: 324,683-328,856 FAM87A
    nsv6828394copy number variation1nstd229human GRCh38 chr8: 365,275-392,820 , GRCh37.p13 chr8: 315,275-342,820 FAM87A
    nsv6827774copy number variation1nstd229human GRCh38 chr8: 375,117-375,746 , GRCh37.p13 chr8: 325,117-325,746 FAM87A
    nsv6826699copy number variation1nstd229human GRCh38 chr8: 320,397-3,564,517 , GRCh37.p13 chr8: 270,397-3,422,039 MIR596, LOC105377781, 33 more genes
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