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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5484682copy number variation1nstd206human GRCh38 chr7: 78,298,508-78,704,406 , GRCh37.p13 chr7: 77,927,825-78,333,722 MAGI2, RPL13AP17, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4825090copy number variation1nstd200human GRCh37 chr7: 77,927,825-78,333,722 , GRCh38.p12 chr7: 78,298,508-78,704,406 RPL13AP17, MAGI2, 1 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4680621copy number variation1nstd189human GRCh37.p13 chr7: 77,843,491-79,282,477 , GRCh38.p12 chr7: 78,214,174-79,653,161 MAGI2, RPL13AP17, 10 more genes
    nsv4675013copy number variation1nstd102humanUncertain significance GRCh37 chr7: 77,500,570-78,015,620 , GRCh38.p12 chr7: 77,871,253-78,386,303 DDX3ILA1, MAGI2, 2 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4139072copy number variation1nstd166human GRCh37.p13 chr7: 77,520,766-78,019,124 , GRCh38.p12 chr7: 77,891,449-78,389,807 DDX3ILA1, RPL13AP17, 2 more genes
    nsv3922762copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112 PMS2P3, RCC1L, 142 more genes
    nsv3921264copy number variation1nstd102humanPathogenic NCBI36 chr7: 74,963,960-77,842,828 , GRCh37 chr7: 75,126,024-78,004,892 , GRCh38 chr7: 75,496,701-78,375,575 PMS2P11, CCDC146, 56 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3919663copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 71,282,013-78,631,323 , GRCh37 chr7: 71,644,077-78,793,387 , GRCh38 chr7: 72,179,092-79,164,071 CLDN4, CLDN3, 149 more genes
    nsv3918722copy number variation1nstd102humanPathogenic GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909 GTF2IP1, POM121, 184 more genes
    nsv3917211copy number variation1nstd102humanPathogenic GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058 HSPB1, UFC1P1, 123 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TRGV3, SNX10-AS1, 2682 more genes
    nsv3902545copy number variation2nstd102humanUncertain significance GRCh37 chr7: 77,522,245-78,019,211 , GRCh38.p12 chr7: 77,892,928-78,389,894 DDX3ILA1, MAGI2, 2 more genes
    nsv3902523copy number variation1nstd102humanPathogenic GRCh37 chr7: 75,588,704-80,277,632 , GRCh38.p12 chr7: 75,959,386-80,648,316 GSAP, POR, 72 more genes
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