btn1a1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	BTN1A1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	BTN1A1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	BTN1A1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	BTN1A1, ITPR3, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	BTN1A1, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	BTN1A1, PRELID1P2, 785 more genes
nsv3877826	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 26,465,768-26,665,235 , GRCh38.p12 chr6: 26,465,540-26,665,007	BTN1A1, TRA-CGC1-1, 23 more genes
nsv3911053	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069	BTN1A1, GPX5, 232 more genes
nsv3872128	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 25,839,165-26,536,884 , GRCh38.p12 chr6: 25,838,937-26,536,656	BTN1A1, HFE-AS1, 78 more genes
nsv4729341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965	BTN1A1, H1-4, 78 more genes
nsv3872893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 26,178,542-26,670,193 , GRCh38.p12 chr6: 26,178,314-26,669,965	BTN1A1, TRX-CAT1-2, 67 more genes
nsv4675256	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 26,256,525-26,536,884 , GRCh38.p12 chr6: 26,256,297-26,536,656	BTN1A1, LOC101928743, 35 more genes
nsv4729472	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 26,345,595-26,601,092 , GRCh38.p12 chr6: 26,345,367-26,600,864	BTN1A1, TRY-GTA6-1, 26 more genes

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btn1a1[All Fields] AND 1[has_clinical] (14)
dbVar
Homo sapiens neurofibromin 2 (NF2), transcript variant 7, mRNA
Homo sapiens neurofibromin 2 (NF2), transcript variant 7, mRNA
gi|163644288|ref|NM_181830.2|

Nucleotide

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