adgrl2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3886439	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 82,263,920-82,313,485 , GRCh38.p12 chr1: 81,798,235-81,847,800	ADGRL2
nsv6314359	complex chromosomal rearrangement	6	nstd102	human	Likely pathogenic	GRCh37 chr1: 81,860,918-81,860,918 , GRCh37 chr1: 81,860,987-81,860,987 , GRCh37 chr1: 97,136,243-97,136,243 , GRCh37 chr1: 106,886,817-106,886,817 , GRCh37 chr10: 56,995,910-56,995,910 , GRCh37 chr14: 29,609,215-29,609,215 , GRCh37 chr1: 97,136,247-97,136,247 , GRCh37 chr1: 106,886,818-106,886,818 , GRCh37 chr14: 29,609,215-29,609,215 , GRCh37 chr4: 38,411,157-38,411,157 , GRCh37 chr4: 38,411,163-38,411,163 , GRCh37 chr10: 56,995,915-56,995,915 , GRCh38.p12 chr1: 81,395,233-81,395,233 , GRCh38.p12 chr1: 81,395,302-81,395,302 , GRCh38.p12 chr1: 106,344,196-106,344,196 , GRCh38.p12 chr14: 29,140,009-29,140,009 , GRCh38.p12 chr14: 29,140,009-29,140,009 , GRCh38.p12 chr1: 96,670,687-96,670,687 , GRCh38.p12 chr1: 106,344,195-106,344,195 , GRCh38.p12 chr4: 38,409,536-38,409,536 , GRCh38.p12 chr10: 55,236,150-55,236,150 , GRCh38.p12 chr10: 55,236,155-55,236,155 , GRCh38.p12 chr1: 96,670,691-96,670,691 , GRCh38.p12 chr4: 38,409,542-38,409,542	ADGRL2, PCDH15, 1 more genes
nsv3901546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611	ADGRL2, ROR1, 333 more genes
nsv6313574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400	ADGRL2, RNA5SP51, 315 more genes
nsv3886551	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986	ADGRL2, RNU6-1102P, 291 more genes
nsv3885743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534	ADGRL2, ZNHIT6, 257 more genes
nsv4454000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657	ADGRL2, NEXN, 209 more genes
nsv3905989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 76,884,987-89,094,147 , NCBI36 chr1: 76,657,575-88,866,735 , GRCh38 chr1: 76,419,302-88,628,464	ADGRL2, DNAJB4, 146 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	ADGRL2, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	ADGRL2, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	ADGRL2, RNU1-153P, 4887 more genes
nsv4728566	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 80,804,502-89,490,384 , GRCh38.p12 chr1: 80,338,817-89,024,701	ADGRL2, CLCA1, 103 more genes
nsv3894725	copy number variation	1	nstd102	human	Benign	GRCh38 chr1: 80,621,564-82,040,802 , NCBI36 chr1: 80,859,837-82,279,074 , GRCh37 chr1: 81,087,249-82,506,486	ADGRL2, RPL10AP4, 11 more genes
nsv7098846	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 81,436,566-81,951,282 , GRCh38.p12 chr1: 80,970,881-81,485,597	ADGRL2, RPL7P10, 6 more genes
nsv3893012	copy number variation	1	nstd102	human	Benign	NCBI36 chr1: 81,209,095-81,696,160 , GRCh37 chr1: 81,436,507-81,923,572 , GRCh38 chr1: 80,970,822-81,457,887	ADGRL2, RPL7P10, 6 more genes
nsv4450384	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 66,085,524-88,429,789 , GRCh38.p12 chr1: 65,619,841-87,964,106	ADGRL2, DEPDC1, 264 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	ADGRL2, LINC01776, 1853 more genes
nsv3906218	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 78,918,729-81,566,060 , GRCh38 chr1: 78,680,456-81,327,787 , GRCh37 chr1: 79,146,141-81,793,472	ADGRL2, RPL7P10, 19 more genes
nsv6313523	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 79,960,197-82,532,594 , GRCh38.p12 chr1: 79,494,512-82,066,910	ADGRL2, RPL7P10, 16 more genes

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adgrl2[All Fields] AND 1[has_clinical] (20)
dbVar
galectin-12 isoform 3 [Homo sapiens]
galectin-12 isoform 3 [Homo sapiens]
gi|216547811|ref|NP_001136008.1|

Protein
Tssr13795 AND (alive[prop]) (0)
Gene

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