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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896132copy number variation1nstd209human GRCh38 chr5: 180,948,146-181,003,606 , GRCh37.p13 chr5: 180,375,146-180,430,606 BTNL3, BTNL8, 3 more genes
    nsv5842266copy number variation1nstd209human GRCh38 chr5: 181,003,508-181,021,905 , GRCh37.p13 chr5: 180,430,508-180,448,905 BTNL3, RNU6-1036P
    nsv5842253copy number variation2nstd209human GRCh38 chr5: 180,987,159-180,994,302 , GRCh37.p13 chr5: 180,414,159-180,421,302 ARPP19P1, BTNL3
    nsv5842252copy number variation2nstd209human GRCh38 chr5: 180,983,359-180,999,481 , GRCh37.p13 chr5: 180,410,359-180,426,481 BTNL3, ARPP19P1
    nsv5580910copy number variation1nstd207human GRCh38 chr5: 180,948,027-181,003,527 , GRCh37.p13 chr5: 180,375,027-180,430,527 BTNL3, BTNL8, 3 more genes
    nsv5556034sequence alteration1nstd206human GRCh38 chr5: 180,989,037-181,073,600 , GRCh37.p13 chr5: 180,416,037-180,500,600 BTNL3, BTNL9, 3 more genes
    nsv5454815copy number variation1nstd206human GRCh38 chr5: 180,948,158-181,003,621 , GRCh37.p13 chr5: 180,375,158-180,430,621 BTNL3, LOC100128762, 3 more genes
    nsv5387223copy number variation1nstd186human GRCh37 chr5: 180,375,528-180,430,689 , GRCh38.p12 chr5: 180,948,528-181,003,689 BTNL3, BTNL8, 3 more genes
    nsv5387170copy number variation1nstd186human GRCh37 chr5: 180,375,155-180,430,666 , GRCh38.p12 chr5: 180,948,155-181,003,666 BTNL3, BTNL8, 3 more genes
    nsv5369118translocation1nstd200human GRCh38 chr5: 180,989,038-180,989,038 , GRCh38 chr5: 181,073,601-181,073,601 , GRCh37.p13 chr5: 180,416,038-180,416,038 , GRCh37.p13 chr5: 180,500,601-180,500,601 BTNL3
    nsv5344199translocation1nstd200human GRCh37 chr5: 180,419,966-180,419,966 , GRCh37 chr5: 180,419,456-180,419,456 , GRCh38.p12 chr5: 180,992,966-180,992,966 , GRCh38.p12 chr5: 180,992,456-180,992,456 BTNL3
    nsv5341751translocation1nstd200human GRCh37 chr5: 180,416,038-180,416,038 , GRCh37 chr5: 180,500,601-180,500,601 , GRCh38.p12 chr5: 180,989,038-180,989,038 , GRCh38.p12 chr5: 181,073,601-181,073,601 BTNL3
    nsv5317062copy number variation1nstd204human GRCh37.p13 chr5: 180,375,062-180,430,579 , GRCh38.p13 chr5: 180,948,062-181,003,579 BTNL3, BTNL8, 3 more genes
    nsv5236213copy number variation1nstd204human GRCh38.p13 chr5: 180,998,601-181,003,700 , GRCh37.p13 chr5: 180,425,601-180,430,700 BTNL3
    nsv5235952copy number variation1nstd204human GRCh38.p13 chr5: 181,002,701-181,003,700 , GRCh37.p13 chr5: 180,429,701-180,430,700 BTNL3
    nsv5235940copy number variation1nstd204human GRCh38.p13 chr5: 180,947,901-181,004,300 , GRCh37.p13 chr5: 180,374,901-180,431,300 BTNL8, ARPP19P1, 3 more genes
    nsv5233409copy number variation1nstd204human GRCh38.p13 chr5: 180,984,001-181,003,700 , GRCh37.p13 chr5: 180,411,001-180,430,700 ARPP19P1, BTNL3
    nsv5231537copy number variation1nstd204human GRCh38.p13 chr5: 180,988,501-180,998,881 , GRCh37.p13 chr5: 180,415,501-180,425,881 BTNL3
    nsv5230004copy number variation1nstd204human GRCh38.p13 chr5: 181,000,901-181,002,700 , GRCh37.p13 chr5: 180,427,901-180,429,700 BTNL3
    nsv5229856copy number variation1nstd204human GRCh38.p13 chr5: 180,948,594-181,001,287 , GRCh37.p13 chr5: 180,375,594-180,428,287 LOC100128762, TMEM69P2, 3 more genes
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