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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979354inversion1nstd209human GRCh38 chr7: 93,906,955-93,907,020 , GRCh37.p13 chr7: 93,536,267-93,536,332 GNGT1
    nsv5569280copy number variation1nstd207human GRCh38 chr7: 93,909,084-93,909,941 , GRCh37.p13 chr7: 93,538,396-93,539,253 GNGT1
    nsv5562484inversion1nstd206human GRCh38 chr7: 93,906,947-93,907,020 , GRCh37.p13 chr7: 93,536,259-93,536,332 GNGT1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487693copy number variation1nstd206human GRCh38 chr7: 93,911,048-93,915,283 , GRCh37.p13 chr7: 93,540,360-93,544,595 GNGT1, LOC105375402
    nsv5477199copy number variation1nstd206human GRCh38 chr7: 93,911,757-93,915,952 , GRCh37.p13 chr7: 93,541,069-93,545,264 LOC105375402, GNGT1
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5321842inversion1nstd204human GRCh38.p13 chr7: 93,906,953-93,907,022 , GRCh37.p13 chr7: 93,536,265-93,536,334 GNGT1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5032629inversion1nstd200human GRCh38 chr7: 93,906,953-93,907,021 , GRCh37.p13 chr7: 93,536,265-93,536,333 GNGT1
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4877956inversion1nstd200human GRCh37 chr7: 93,536,266-93,536,334 , GRCh38.p12 chr7: 93,906,954-93,907,022 GNGT1
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729505copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,209,718-94,202,220 , GRCh38.p12 chr7: 93,580,406-94,572,908 LOC105375404, GNG11, 15 more genes
    nsv4715619copy number variation1nstd195human GRCh37 chr7: 93,422,601-93,787,501 , GRCh38.p12 chr7: 93,793,289-94,158,189 , GNG11, 7 more genes
    nsv4709072inversion1nstd195human GRCh37 chr7: 93,534,899-93,534,900 , GRCh38.p12 chr7: 93,905,587-93,905,588 GNGT1
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 LOC105375404, BET1, 36 more genes
    nsv4455688copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,332,477-93,546,008 , GRCh38.p12 chr7: 93,703,165-93,916,696 TFPI2, TFPI2-DT, 4 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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