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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7045314inversion1nstd229human GRCh38 chr6: 130,549,578-131,340,236 , GRCh37.p13 chr6: 130,870,723-131,661,376 AKAP7, LOC100421246, 6 more genes
    nsv7042993inversion1nstd229human GRCh38 chr6: 130,553,332-131,340,232 , GRCh37.p13 chr6: 130,874,477-131,661,372 AKAP7, LOC105378004, 6 more genes
    nsv7039138inversion1nstd229human GRCh38 chr6: 130,671,952-130,834,227 , GRCh37.p13 chr6: 130,993,097-131,155,367 SMLR1, LOC105378002, 2 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6813665copy number variation1nstd229human GRCh38 chr6: 130,617,784-130,887,930 , GRCh37.p13 chr6: 130,938,929-131,209,070 EPB41L2, LOC105378002, 2 more genes
    nsv6809778copy number variation1nstd229human GRCh38 chr6: 130,730,901-130,836,200 , GRCh37.p13 chr6: 131,052,046-131,157,340 EPB41L2, SMLR1, 1 more genes
    nsv6808420copy number variation1nstd229human GRCh38 chr6: 130,549,501-131,568,700 , GRCh37.p13 chr6: 130,870,646-131,889,840 LOC105378002, LOC105378005, 8 more genes
    nsv6805287copy number variation1nstd229human GRCh38 chr6: 130,713,095-130,834,226 , GRCh37.p13 chr6: 131,034,240-131,155,366 LOC105378003, SMLR1, 2 more genes
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6313685copy number variation1nstd102humanUncertain significance GRCh37 chr6: 130,949,600-131,924,268 , GRCh38.p12 chr6: 130,628,455-131,603,128 ARG1, LOC100421246, 10 more genes
    nsv6290946copy number variation1nstd102humanPathogenic GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079 LOC105378004, LINC01010, 89 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5553035insertion1nstd206human GRCh38 chr6: 130,837,414-130,837,448 , GRCh37.p13 chr6: 131,158,554-131,158,588 SMLR1, EPB41L2
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4349636copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 129,513,837-132,618,991 , GRCh38.p12 chr6: 129,192,692-132,297,852 ARG1, CCN2, 37 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
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