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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901540copy number variation1nstd209human GRCh38 chr6: 10,946,336-10,946,394 , GRCh37.p13 chr6: 10,946,569-10,946,627 SYCP2L, LOC101928191
    nsv5725700mobile element insertion1nstd211human GRCh38 chr6: 10,942,787-10,942,787 , GRCh37.p13 chr6: 10,943,020-10,943,020 SYCP2L, LOC101928191
    nsv5693372mobile element insertion2nstd211human GRCh38 chr6: 10,941,945-10,941,945 , GRCh37.p13 chr6: 10,942,178-10,942,178 SYCP2L, LOC101928191
    nsv5398179mobile element insertion1nstd206human GRCh38 chr6: 10,941,945-10,941,996 , GRCh37.p13 chr6: 10,942,178-10,942,229 LOC101928191, SYCP2L
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4932695copy number variation1nstd200human GRCh38 chr6: 10,938,890-10,940,174 , GRCh37.p13 chr6: 10,939,123-10,940,407 LOC101928191, SYCP2L
    nsv4809702copy number variation1nstd200human GRCh37 chr6: 10,890,139-10,972,111 , GRCh38.p12 chr6: 10,889,906-10,971,878 LOC101928191, SYCP2L
    nsv4683407copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,393,732-11,011,042 , GRCh38.p12 chr6: 10,393,499-11,010,809 MAK, TMEM14C, 22 more genes
    nsv4665634copy number variation2nstd186human GRCh37 chr6: 10,954,299-10,954,344 , GRCh38.p12 chr6: 10,954,066-10,954,111 SYCP2L, LOC101928191
    nsv4591969copy number variation2nstd183human GRCh37 chr6: 10,954,299-10,954,344 , GRCh38.p12 chr6: 10,954,066-10,954,111 LOC101928191, SYCP2L
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4113756copy number variation1nstd166human GRCh37.p13 chr6: 10,939,123-10,940,407 , GRCh38.p12 chr6: 10,938,890-10,940,174 LOC101928191, SYCP2L
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 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 PRELID1P2, RPL7AP7, 785 more genes
    nsv3918645copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817 BMP6, BPHL, 194 more genes
    nsv3918220copy number variation1nstd102humanPathogenic GRCh38 chr6: 10,601,499-13,987,316 , NCBI36 chr6: 10,709,718-14,095,526 , GRCh37 chr6: 10,601,732-13,987,547 GCNT2, LOC105374935, 58 more genes
    nsv3914672copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-13,189,419 , GRCh37 chr6: 156,974-13,081,433 , GRCh38 chr6: 156,974-13,081,201 BMP6, BPHL, 212 more genes
    nsv3914068copy number variation1nstd102humanPathogenic NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031 SSR1, LOC107986560, 145 more genes
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