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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4728934copy number variation1nstd102humanUncertain significance GRCh37 chr6: 16,928,560-17,132,863 , GRCh38.p12 chr6: 16,928,329-17,132,632 STMND1, LOC107986573, 2 more genes
    nsv3872373copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,354,402-17,950,079 , GRCh38.p12 chr6: 5,354,169-17,949,848 STMND1, TMEM14B, 189 more genes
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 STMND1, SOX4, 136 more genes
    nsv3875604copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,693,852-24,225,515 , GRCh38.p12 chr6: 13,693,620-24,225,287 STMND1, KIF13A, 124 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 STMND1, LOC101928354, 101 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 STMND1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 STMND1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 STMND1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 STMND1, ITPR3, 2905 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 STMND1, TRR-ACG1-2, 1385 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 STMND1, PRELID1P2, 785 more genes
    nsv3888615copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006 STMND1, LOC107986557, 349 more genes
    nsv3872568copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006 STMND1, TXNDC5, 349 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 STMND1, LOC105374960, 342 more genes
    nsv3886069copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-21,955,964 , GRCh38.p12 chr6: 156,974-21,955,733 STMND1, FOXCUT, 331 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 STMND1, LOC101928354, 321 more genes
    nsv3913657copy number variation1nstd102humanPathogenic NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826 STMND1, LOC105374904, 294 more genes
    nsv3915452copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 14,838,766-17,662,301 , GRCh37 chr6: 14,730,787-17,554,322 , GRCh38 chr6: 14,730,556-17,554,091 STMND1, GMPR, 32 more genes
    nsv3883690copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 8,269,414-17,402,660 , GRCh38.p12 chr6: 8,269,181-17,402,429 STMND1, EDN1, 129 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 STMND1, RNU6-522P, 70 more genes
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