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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 TRPV6, RNU6-438P, 2682 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 TRPV6, ATG9B, 603 more genes
    nsv3915633copy number variation1nstd102humanPathogenic NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574 TRPV6, MOXD2P, 561 more genes
    nsv3897512copy number variation1nstd102humanPathogenic GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017 TRPV6, LOC105375548, 520 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 TRPV6, NOBOX, 466 more genes
    nsv3903590copy number variation1nstd102humanPathogenic GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080 TRPV6, LOC105375597, 468 more genes
    nsv3910344copy number variation1nstd102humanPathogenic GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973 TRPV6, LOC112268012, 461 more genes
    nsv3905379copy number variation1nstd102humanPathogenic GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017 TRPV6, AGAP3, 459 more genes
    nsv3919772copy number variation1nstd102humanPathogenic NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866 TRPV6, LOC105375567, 429 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRPV6, TRBD2, 403 more genes
    nsv3904188copy number variation1nstd102humanPathogenic GRCh37 chr7: 141,938,235-159,126,310 , GRCh38.p12 chr7: 142,288,582-159,333,620 TRPV6, RBM33-DT, 423 more genes
    nsv3914137copy number variation1nstd102humanPathogenic GRCh37 chr7: 134,702,438-148,504,492 , NCBI36 chr7: 134,352,978-148,135,425 , GRCh38 chr7: 135,017,687-148,807,400 TRPV6, FAM180A, 348 more genes
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRPV6, TRBJ2-7, 341 more genes
    nsv3910067copy number variation1nstd102humanPathogenic GRCh38 chr7: 135,414,108-144,140,219 , NCBI36 chr7: 134,749,397-143,468,245 , GRCh37 chr7: 135,098,857-143,837,312 TRPV6, LOC105375534, 292 more genes
    nsv3920625copy number variation1nstd102humanPathogenic GRCh38 chr7: 142,578,948-144,254,897 , NCBI36 chr7: 141,967,554-143,582,923 , GRCh37 chr7: 142,528,609-143,951,990 TRPV6, OR2A14, 120 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 TRPV6, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 TRPV6, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 TRPV6, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TRPV6, TRGV3, 2682 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 TRPV6, SEPTIN7P6, 1175 more genes
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