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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7021776copy number variation1nstd229human GRCh38 chr22: 21,649,871-21,655,208 , GRCh37.p13 chr22: 22,004,160-22,009,497 MIR301B, MIR130B
    nsv6637518copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,029,656-22,485,776 , GRCh38.p12 chr22: 20,675,368-22,131,383 ABHD17AP5, MIR301B, 70 more genes
    nsv6637335copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,662-22,962,962 , GRCh38.p12 chr22: 21,111,373-22,620,492 ABHD17AP5, UBE2L3, 97 more genes
    nsv6627184copy number variation1nstd224human GRCh37 chr22: 21,799,719-23,803,722 , GRCh38.p12 chr22: 21,445,430-23,461,535 BCRP4, GNAZ, 158 more genes
    nsv6540095copy number variation1nstd223human GRCh38 chr22: 20,268,331-23,402,807 , GRCh37.p13 chr22: 20,255,854-23,744,994 IGLC2, IGLVIV-53, 214 more genes
    nsv6539225copy number variation1nstd223human GRCh38 chr22: 21,602,489-21,697,311 , GRCh37.p13 chr22: 21,956,778-22,051,600 PPIL2, YDJC, 7 more genes
    nsv6315562copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,798,906-25,039,018 , GRCh38.p12 chr22: 21,444,617-24,643,051 IGLVI-42, ADORA2A-AS1, 205 more genes
    nsv6315480copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,462,566-22,962,196 , GRCh38.p12 chr22: 21,108,277-22,619,726 IGLV8-61, SDF2L1, 97 more genes
    nsv6315191copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,322,233-22,065,138 , GRCh38.p12 chr22: 20,967,945-21,710,849 TUBA3GP, MIR649, 39 more genes
    nsv6314782copy number variation1nstd220human GRCh38.p12 chr22: 21,351,861-24,248,764 , GRCh37 chr22: 21,706,150-24,644,732 ASLP1, BCR, 195 more genes
    nsv6291785copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,974,641-22,401,879 , GRCh38.p12 chr22: 21,620,352-22,047,481 IGL, CCDC116, 19 more genes
    nsv6291464copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,661-24,631,791 , GRCh38.p12 chr22: 21,111,372-24,235,823 IGLVIV-64, FAM230B, 205 more genes
    nsv6290344copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,905,051-22,989,041 , GRCh38.p12 chr22: 21,550,762-22,646,571 IGLV1-47, LOC100736408, 81 more genes
    nsv6289929copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,514,655-22,986,816 , GRCh38.p12 chr22: 21,160,366-22,644,345 IGLV9-49, BCRP6, 97 more genes
    nsv6134584copy number variation1nstd213human GRCh37 chr22: 21,970,000-27,770,001 , GRCh38.p12 chr22: 21,615,711-27,374,040 ADORA2A, GRK3, 259 more genes
    nsv6102002inversion1nstd212human GRCh38 chr22: 20,753,977-24,184,938 , GRCh37.p13 chr22: 21,108,265-24,580,906 , ASLP1, 226 more genes
    nsv5292718copy number variation1nstd204human GRCh38.p13 chr22: 21,640,542-21,655,304 , GRCh37.p13 chr22: 21,994,831-22,009,593 LOC107985532, SDF2L1, 2 more genes
    nsv5288765copy number variation1nstd204human GRCh38.p13 chr22: 21,649,338-21,668,728 , GRCh37.p13 chr22: 22,003,627-22,023,017 LOC107985532, PPIL2, 2 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4730001copy number variation1nstd102humanPathogenic GRCh37 chr22: 19,035,089-22,672,555 , GRCh38.p12 chr22: 18,339,130-22,318,200 C22orf39, IGLL4P, 191 more genes
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