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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4631532copy number variation1nstd183human GRCh37 chr22: 17,308,484-17,312,646 , GRCh38.p12 chr22: 16,827,594-16,831,756 HSFY1P1
    esv23434sequence alteration1estd20human NCBI36 chr22: 15,688,484-15,692,646 , GRCh37.p13 chr22: 17,308,484-17,312,646 , GRCh38.p12 chr22: 16,827,594-16,831,756 HSFY1P1
    esv13059copy number variation1estd20human NCBI36 chr22: 15,688,484-15,692,646 , GRCh37.p13 chr22: 17,308,484-17,312,646 , GRCh38.p12 chr22: 16,827,594-16,831,756 HSFY1P1
    esv1483418copy number variation1estd22human NCBI36 chr22: 15,687,812-15,687,816 , GRCh37.p13 chr22: 17,307,812-17,307,816 , GRCh38.p12 chr22: 16,826,922-16,826,926 HSFY1P1
    nsv4288899copy number variation1nstd166human GRCh37.p13 chr22: 17,307,000-17,312,000 , GRCh38.p12 chr22: 16,826,110-16,831,110 HSFY1P1
    nsv4509448mobile element insertion1nstd166human GRCh37.p13 chr22: 17,307,076-17,307,076 , GRCh38.p12 chr22: 16,826,186-16,826,186 HSFY1P1
    esv2978230insertion1estd209human GRCh37 chr22: 17,309,257-17,309,257 , GRCh38.p12 chr22: 16,828,367-16,828,367 HSFY1P1
    esv2978229insertion1estd209human GRCh37 chr22: 17,306,941-17,306,941 , GRCh38.p12 chr22: 16,826,051-16,826,051 HSFY1P1
    esv2496040insertion1estd197human NCBI36 chr22: 15,686,942-15,686,942 , GRCh37.p13 chr22: 17,306,942-17,306,942 , GRCh38.p12 chr22: 16,826,052-16,826,052 HSFY1P1
    esv2179751insertion1estd194human NCBI36 chr22: 15,689,258-15,689,258 , GRCh37.p13 chr22: 17,309,258-17,309,258 , GRCh38.p12 chr22: 16,828,368-16,828,368 HSFY1P1
    esv2107061insertion1estd194human NCBI36 chr22: 15,686,942-15,686,942 , GRCh37.p13 chr22: 17,306,942-17,306,942 , GRCh38.p12 chr22: 16,826,052-16,826,052 HSFY1P1
    esv1493866insertion1estd22human NCBI36 chr22: 15,686,943-15,686,943 , GRCh37.p13 chr22: 17,306,943-17,306,943 , GRCh38.p12 chr22: 16,826,053-16,826,053 HSFY1P1
    nsv2136839short tandem repeat7nstd128human GRCh37 chr22: 17,307,814-17,307,852 , GRCh38.p12 chr22: 16,826,924-16,826,962 HSFY1P1
    nsv6627169copy number variation1nstd224human GRCh37 chr22: 17,301,217-17,329,601 , GRCh38.p12 chr22: 16,820,327-16,848,711 HSFY1P1, GPM6BP3, 1 more genes
    nsv3161337copy number variation1nstd151human GRCh37 chr22: 17,264,506-17,385,613 , GRCh38.p12 chr22: 16,783,616-16,904,723 XKR3, GPM6BP3, 3 more genes
    esv3568223copy number variation1estd212human GRCh37 chr22: 17,279,115-17,330,095 , GRCh38.p12 chr22: 16,798,225-16,849,205 HSFY1P1, XKR3, 1 more genes
    nsv588081copy number variation1nstd54human NCBI36 chr22: 15,634,399-15,706,181 , GRCh37.p13 chr22: 17,254,399-17,326,181 , GRCh38.p12 chr22: 16,773,509-16,845,291 XKR3, GPM6BP3, 1 more genes
    nsv588083copy number variation1nstd54human NCBI36 chr22: 15,674,251-15,706,432 , GRCh37.p13 chr22: 17,294,251-17,326,432 , GRCh38.p12 chr22: 16,813,361-16,845,542 GPM6BP3, HSFY1P1, 1 more genes
    nsv588084copy number variation1nstd54human NCBI36 chr22: 15,681,217-15,699,156 , GRCh37.p13 chr22: 17,301,217-17,319,156 , GRCh38.p12 chr22: 16,820,327-16,838,266 HSFY1P1, XKR3, 1 more genes
    nsv459334copy number variation1nstd27human NCBI35 chr22: 15,668,805-15,700,986 , GRCh37.p13 chr22: 17,294,251-17,326,432 , GRCh38.p12 chr22: 16,813,361-16,845,542 XKR3, HSFY1P1, 1 more genes
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