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Items: 1 to 20 of 151

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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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964848copy number variation1nstd200human GRCh38 chr7: 76,290,829-76,301,780 , GRCh37.p13 chr7: 75,921,849-75,931,097 HSPB1
    nsv4950142copy number variation1nstd200human GRCh38 chr7: 76,303,434-76,306,017 , GRCh37.p13 chr7: 75,932,751-75,935,334 HSPB1
    nsv4825080copy number variation1nstd200human GRCh37 chr7: 75,920,126-75,931,093 , GRCh38.p12 chr7: 76,290,809-76,301,776 HSPB1
    nsv4811971copy number variation1nstd200human GRCh37 chr7: 75,932,761-75,935,332 , GRCh38.p12 chr7: 76,303,444-76,306,015 HSPB1
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 FDPSP7, LOC105375352, 119 more genes
    nsv4682984copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,930,759-75,933,500 , GRCh38.p12 chr7: 76,301,442-76,304,183 HSPB1
    nsv4682663copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,914,933-76,029,908 , GRCh38.p12 chr7: 76,285,615-76,400,591 ZP3, YWHAG, 3 more genes
    nsv4682391copy number variation1nstd102humanPathogenic GRCh37 chr7: 75,933,106-75,933,500 , GRCh38.p12 chr7: 76,303,789-76,304,183 HSPB1
    nsv4680300copy number variation1nstd189human GRCh37.p13 chr7: 75,220,394-75,956,150 , GRCh38.p12 chr7: 75,591,076-76,326,833 HIP1, HSPB1, 18 more genes
    nsv4675200copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063 PHB1P15, FKBP6P2, 87 more genes
    nsv4607143copy number variation1nstd183human GRCh37 chr7: 75,859,030-75,935,056 , GRCh38.p12 chr7: 76,229,712-76,305,739 HSPB1, SRRM3
    nsv4525174copy number variation1nstd166human GRCh37.p13 chr7: 75,932,762-75,935,344 , GRCh38.p12 chr7: 76,303,445-76,306,027 HSPB1
    nsv4457107copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,076,890-76,007,283 , GRCh38.p12 chr7: 75,447,619-76,377,966 CCL24, RPL7L1P3, 21 more genes
    nsv4456710copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,748,898-75,981,782 , GRCh38.p12 chr7: 76,119,580-76,352,465 YWHAG, LOC100996476, 3 more genes
    nsv4455881copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,233,243-76,007,283 , GRCh38.p12 chr7: 75,603,925-76,377,966 RHBDD2, MIR4651, 18 more genes
    nsv4455498copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,091,878-76,117,614 , GRCh38.p12 chr7: 75,462,613-76,488,297 SPDYE5, HIP1, 25 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
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